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Trial registered on ANZCTR
Registration number
ACTRN12611001095954
Ethics application status
Approved
Date submitted
19/10/2011
Date registered
21/10/2011
Date last updated
21/10/2011
Type of registration
Retrospectively registered
Titles & IDs
Public title
Treatment of chronic refractory urticaria with the medicine adalimumab
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Scientific title
Treatment of chronic refractory urticaria with adalimumab
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Secondary ID [1]
273231
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Nil known
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Universal Trial Number (UTN)
U1111-1125-3242
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Urticaria
278991
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Condition category
Condition code
Skin
279173
279173
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0
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Dermatological conditions
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment with adalimumab
Dose: 80 mg at first administration week 0, thereafter 40 mg at week 1+3+5+7+9+11+13+15.
Total duration af treatment is 16 weeks.
The mode of administration is subcutaneous.
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Intervention code [1]
269563
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Treatment: Drugs
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Comparator / control treatment
Uncontrolled study
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
279810
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Urticaria Activity Score
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Assessment method [1]
279810
0
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Timepoint [1]
279810
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Baseline and week 4, 9, 16, 18, 20 and 28
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Secondary outcome [1]
294496
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Itch assessed with Structured Itch Questionnaire
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Assessment method [1]
294496
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Timepoint [1]
294496
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Baseline and week 4, 9, 16, 18, 20 and 28
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Secondary outcome [2]
294497
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Life quality and emotions assessed with Becks Depression Inventory, Brief Symptom Inventory and Dermatology Life Quality Index
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Assessment method [2]
294497
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Timepoint [2]
294497
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Baseline and week 4, 9, 16, 18, 20 and 28
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Secondary outcome [3]
294498
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Sleep quality assessed with Pittsburg Sleep Quality Index
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Assessment method [3]
294498
0
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Timepoint [3]
294498
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Baseline and week 4, 9, 16, 18, 20 and 28
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Secondary outcome [4]
294499
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Bodily sensations assessed with Somatosensory Amplification Scale
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Assessment method [4]
294499
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Timepoint [4]
294499
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Baseline and week 4, 9, 16, 18, 20 and 28
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Eligibility
Key inclusion criteria
Patients with chronic urticaria. Duration of chronic urticaria more than 6 months with maximum 2 days between urticaria outbreaks. Unsatisfactory treatment with high dose antihistamines, prednisolone and at least one other immunosuppressive drug for at least 3 months. Unsatisfactory treatment is defined as symptoms several times at week despite treatment.
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Minimum age
18
Years
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Maximum age
67
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Pregnancy and lactation
Diabetes Mellitus
Severe heart disease, kidney disease or liver disease
Chronic infections
Former malignancies except non-melanoma skin cancer
Former treatment with tumour necrosis factor alpha-inhibitors
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
Phase 4
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
1/08/2011
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
10
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
3914
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Denmark
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State/province [1]
3914
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Funding & Sponsors
Funding source category [1]
270060
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Commercial sector/Industry
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Name [1]
270060
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Abbott Denmark
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Address [1]
270060
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Emdrupvej 28C
2100 Koebenhavn Oe
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Country [1]
270060
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Denmark
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Funding source category [2]
270061
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Charities/Societies/Foundations
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Name [2]
270061
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Aage Bang Foundation
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Address [2]
270061
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Frederiksgade 19, 4
1265 Koebenhavn K
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Country [2]
270061
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Denmark
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Primary sponsor type
Individual
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Name
Senior doctor Claus Zachariae
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Address
Niels Andersens Vej 65
2900 Hellerup
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Country
Denmark
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Secondary sponsor category [1]
269024
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None
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Name [1]
269024
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Address [1]
269024
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Country [1]
269024
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
272017
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Ethics Committee of the Capital Region of Denmark
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Ethics committee address [1]
272017
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Kongens Vaenge 2 3400 Hilleroed
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Ethics committee country [1]
272017
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Denmark
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Date submitted for ethics approval [1]
272017
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Approval date [1]
272017
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Ethics approval number [1]
272017
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Summary
Brief summary
The purpose of the study is to examine, whether patients with longlasting urticaria, where other treatments have been ineffective, will benefit from treatment with the drug adalimumab. The cytokine tumour necrosis factor alfa is upregulated in the skin and serum in patients with urticaria. Adalimumab is a drug, that blocks tumour necrosis factor alfa.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
33280
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Address
33280
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Country
33280
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Phone
33280
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Fax
33280
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Email
33280
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Contact person for public queries
Name
16527
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Claus Zachariae
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Address
16527
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Niels Andersens Vej 65
2900 Hellerup
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Country
16527
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Denmark
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Phone
16527
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+45 3977 3203
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Fax
16527
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Email
16527
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[email protected]
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Contact person for scientific queries
Name
7455
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Claus Zachariae
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Address
7455
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Niels Andersens Vej 65
2900 Hellerup
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Country
7455
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Denmark
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Phone
7455
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+45 3977 3203
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Fax
7455
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Email
7455
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[email protected]
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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
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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