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Trial registered on ANZCTR
Registration number
ACTRN12611000122954
Ethics application status
Approved
Date submitted
13/07/2010
Date registered
3/02/2011
Date last updated
18/06/2014
Type of registration
Retrospectively registered
Titles & IDs
Public title
Evaluation of pulmonary function conditions pre-radiotherapy in breast cancer treatment.
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Scientific title
A single group study on early detection of functional pulmonary loss before radiotherapy on breast cancer patients.
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Secondary ID [1]
252197
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Nil.
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Universal Trial Number (UTN)
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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:
Functional pulmonary loss.
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Breast cancer.
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Condition category
Condition code
Cancer
257903
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0
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Breast
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Respiratory
257904
257904
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0
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Other respiratory disorders / diseases
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The patients’ pulmonary function was evaluated immediately before they were submitted to radiotherapy, using clinical instruments, such as incentive spirometers, manuvacuometer, peak flow, and six minute walk test. Each patient was assessed once only and the duration of the evaluation was thirty minutes.
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Intervention code [1]
256792
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Early detection / Screening
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Comparator / control treatment
N/A this is a single group study. Each patient’s pulmonary function was compared to their own normative value.
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Primary Outcome: loss of pulmonary function evaluated with incentive spirometers (IC, FVC), manuvacuometer (Pimax and Pemax.), peak flow (FP).
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Assessment method [1]
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Timepoint [1]
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Timepoint: immediately before radiotherapy.
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Secondary outcome [1]
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Secondary Outcome: comparing chemotherapy adjuvant and neoadjuvant influence in loss of pulmonary function evaluated with incentive spirometers (IC, FVC), manuvacuometer (Pimax and Pemax.), peak flow (FP).
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Assessment method [1]
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Timepoint [1]
264825
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Timepoint: immediately before radiotherapy.
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Eligibility
Key inclusion criteria
Documented breast cancer diagnosis, operated, with radiotherapy proposition as an adjuvant treatment, after chemotherapy and/or hormone therapy neoadjuvant or adjuvant, no past or present clinical evidence of benign or malign pulmonary disease based on oncological follow up and previous history and cognitive capacity to understand simple commands and to execute tasks during testing.
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Minimum age
35
Years
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Maximum age
No limit
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Women who were submitted to radiotherapy concomitant to chemotherapy were excluded from the study.
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Study design
Purpose of the study
Diagnosis
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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
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
22/04/2008
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Actual
22/04/2008
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Date of last participant enrolment
Anticipated
23/06/2009
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Actual
23/06/2009
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
36
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
2758
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Brazil
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State/province [1]
2758
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Minas Gerais (MG)
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Funding & Sponsors
Funding source category [1]
257278
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Self funded/Unfunded
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Name [1]
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unfunded
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Address [1]
257278
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Country [1]
257278
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Primary sponsor type
Individual
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Name
Renata de Carvalho Schettino
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Address
Matipo street, 177/202 Santo Antonio cep:30350-210
BH-MG
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Country
Brazil
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Secondary sponsor category [1]
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Individual
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Name [1]
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Karla de Carvalho Schettino
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Address [1]
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Matipo street, 177/202 Santo Antonio cep:30350-210
BH-MG
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Country [1]
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Brazil
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Secondary sponsor category [2]
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Individual
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Name [2]
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Geovanni Dantas Cassali
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Address [2]
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Av. Pres. Antonio Carlos 6627 Pampulha- Instituto de Ciencias Biologicas- Cep: 31270-901 BH-MG
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Country [2]
256521
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Brazil
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Other collaborator category [1]
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Individual
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Name [1]
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Miguel Torres Teixeira Leite
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Address [1]
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Av. Pres. Antonio Carlos 6627 Pampulha- Instituto de Ciencias Biologicas- Cep: 31270-901 BH-MG
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Country [1]
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Brazil
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Comite de etica em pesquisa da Universidade Federal de Minas Gerais - COEP UFMG
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Ethics committee address [1]
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Av. Pres. Antonio Carlos 6627 Pampulha unidade Administrativa II sala 2005 Cep: 31270-901 BH-MG
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Ethics committee country [1]
260393
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Brazil
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Date submitted for ethics approval [1]
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29/11/2007
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Approval date [1]
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16/04/2008
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Ethics approval number [1]
260393
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ETIC CAAE-0605.0.203.000-07
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Summary
Brief summary
The aim of this study was to transversally detect, by means of routinely used physiotherapeutic instruments and a functional test, alterations in pulmonary functions due to the systemic treatments pre-radiotherapy in breast cancer treatment. Women submitted to breast cancer systemic treatments show a decrease in pulmonary function, which impairs their respiratory conditions pre-radiotherapy.
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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
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Mrs Renata de Carvalho Schettino
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Address
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Universidade Federal de Minas Gerais (UFMG)
Rua Matipo 177/202
Bairro Santo Antonio
BH-MG
CEP 30350210
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Country
31385
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Brazil
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Phone
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+55 31 33441161
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Fax
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+55 31 34092879
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Email
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[email protected]
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Contact person for public queries
Name
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Renata de Carvalho Schettino
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Address
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Matipo street, 177/202 Santo Antonio Cep:30350-210 BH-MG
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Country
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Brazil
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Phone
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+55 31 33441161
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Fax
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+55 31 34092879
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Email
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[email protected]
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Contact person for scientific queries
Name
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Renata de Carvalho Schettino
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Address
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Matipo street, 177/202 Santo Antonio Cep:30350-210 BH-MG
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Country
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Brazil
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Phone
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+55 31 33441161
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Fax
5560
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+55 31 34092879
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Email
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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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