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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT00366249




Registration number
NCT00366249
Ethics application status
Date submitted
17/08/2006
Date registered
21/08/2006
Date last updated
28/04/2010

Titles & IDs
Public title
Study Evaluating the Safety and Efficacy of a Once-daily Dose of Tigecycline vs Ertapenem in Diabetic Foot Infections (DFI) With a Substudy in Patients With Diabetic Foot Infections Complicated by Osteomyelitis.
Scientific title
A Multicenter, Randomized, Double-Blind, Comparison Study of the Safety and Efficacy of a Once-Daily Dose of Tigecycline Versus Ertapenem for the Treatment of Foot Infections in Subjects With Diabetes
Secondary ID [1] 0 0
3074K5-319
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Bacterial Infections 0 0
Diabetic Foot 0 0
Osteomyelitis 0 0
Condition category
Condition code
Infection 0 0 0 0
Studies of infection and infectious agents
Infection 0 0 0 0
Other infectious diseases
Infection 0 0 0 0
Sexually transmitted infections
Musculoskeletal 0 0 0 0
Other muscular and skeletal disorders
Inflammatory and Immune System 0 0 0 0
Other inflammatory or immune system disorders
Metabolic and Endocrine 0 0 0 0
Diabetes

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - Tigecycline
Treatment: Drugs - Ertapenem

Active comparator: A -

Active comparator: B -


Treatment: Drugs: Tigecycline
150 mg Tigecycline once-daily IV infusion for up to 28 days, or 42 days for the substudy wth osteomyelitis

Treatment: Drugs: Ertapenem
Ertapenem 1g IV infusion every 24 hours +/- vancomycin depending on culture results and at the discretion of investigator (for coverage of Methicillin-resistant Staphylococcus aureus (MRSA), coagulase-negative staphylococci (CNS) or enterococci coverage).
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Number of Patients With Clinical Response of Cure Vs. Failure.
Timepoint [1] 0 0
Test of cure visit (TOC): Assessed at least 12 days post last dose
Primary outcome [2] 0 0
Number of Patients With Clinical Response of Cure Vs. Failure/Indeterminate.
Timepoint [2] 0 0
Test of cure visit (TOC): Assessed at least 12 days post last dose
Secondary outcome [1] 0 0
Number of Patients With Clinical Response of Cure Vs. Failure Assessed at Least 25 - 27 Weeks Post Last Dose.
Timepoint [1] 0 0
Test of cure visit (TOC): Assessed at least 25 - 27 weeks post last dose
Secondary outcome [2] 0 0
Number of Patients With Clinical Response of Cure Vs. Failure/Indeterminate Assessed at Least 25 - 27 Weeks Post Last Dose.
Timepoint [2] 0 0
Test of cure visit (TOC): Assessed at least 25 - 27 weeks post last dose
Secondary outcome [3] 0 0
Number of Patients With Microbiologic Response of Eradication.
Timepoint [3] 0 0
Test of cure visit (TOC): Assessed at least 12 days post last dose

Eligibility
Key inclusion criteria
Main inclusion criteria:

* Men and women aged 18 or older with diabetes and a qualifying foot infection. People with evidence of a diabetic foot infection with osteomyelitis may qualify for the osteomyelitis substudy arm.

Main exclusion criteria:

* People with additional significant disease, infection with resistant pathogens, contraindication, or hypersensitivity to any test article or related antibiotic.
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s

The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 3
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
1/01/2007
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
1/03/2009
Sample size
Target
Accrual to date
Final
1061
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 0 0
- Melbourne
Recruitment postcode(s) [1] 0 0
3050 - Melbourne
Recruitment postcode(s) [2] 0 0
3128 - Melbourne
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
California
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United States of America
State/province [2] 0 0
Florida
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United States of America
State/province [3] 0 0
Hawaii
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United States of America
State/province [4] 0 0
Illinois
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United States of America
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Maryland
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United States of America
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Massachusetts
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United States of America
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New Jersey
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North Carolina
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United States of America
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Ohio
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United States of America
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Pennsylvania
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United States of America
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South Carolina
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United States of America
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Texas
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Argentina
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Buenos Aires
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Argentina
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Entre Rios
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Argentina
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Entre Ríos
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Argentina
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Mendoza
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Argentina
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Provincia de Buenos Aires
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Argentina
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Provincia de Tucuman
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Argentina
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Santa Fe
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Argentina
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Ciudad Autonoma de Buenos Aires
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Argentina
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Cordoba
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Austria
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Wien
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Belgium
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Bornem
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Belgium
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Brussel
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Belgium
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Bruxelles
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Belgium
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Pellenberg
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Brazil
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Rio de Janeiro
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Brazil
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Sao Paulo
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Canada
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British Columbia
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Canada
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Manitoba
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Canada
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Ontario
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Canada
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Quebec
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Chile
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Santiago
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Chile
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Valdivia
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China
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Heilongjiang
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China
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Beijing
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China
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Guangzhou
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China
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Tianjin
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Colombia
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Bogota
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Croatia
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Zadar
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Croatia
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Zagreb
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Denmark
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Odense
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Estonia
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Ida Virumaa
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Estonia
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Tallinn
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Estonia
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Tartu
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Finland
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Kuopio
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Finland
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Turku
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France
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Strasbourg
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France
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Tourcoing
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Germany
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Hessen
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Germany
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North Rhine-Westphalia
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Germany
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Northrhien-Westphalia
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Greece
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Athens
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Greece
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Holargos, Athens
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Greece
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Rio-Patras
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Budapest
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Debrecen
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Gyor
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Kistarcsa
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Hungary
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Szekesfehervar
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Gujarat
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Maharashtra
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Abano terme (PD)
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Pisa
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Seoul
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Liepaja
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Lithuania
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Panevezys
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Lithuania
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Siauliai
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Lithuania
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Vilnius
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Mexico
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Jalisco
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Durango
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San Luis Potosi
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Lima
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Wroclaw
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Bacau
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Romania
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Bucharest
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Romania
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Cluj-Napoca
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Romania
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Lasi
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Kemerovo
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Russian Federation
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Taoyuan Hsien
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Adana
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Capa-Istanbul
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Istanbul
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Ukraine
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Cherkassy
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Dnepropetrovsk
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Ukraine
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Kiev
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Ukraine
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Kyiv
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Ukraine
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Lviv
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Ukraine
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Vinnytsia
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Ukraine
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Zaporozhye
Country [141] 0 0
United Kingdom
State/province [141] 0 0
Lanarkshire
Country [142] 0 0
United Kingdom
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West Midlands
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United Kingdom
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Birmingham
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United Kingdom
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London
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United Kingdom
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Oxford

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Wyeth is now a wholly owned subsidiary of Pfizer
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Medical Monitor
Address 0 0
Wyeth is now a wholly owned subsidiary of Pfizer
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.

Results are available at https://clinicaltrials.gov/study/NCT00366249