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Trial registered on ANZCTR
Registration number
ACTRN12612001006831
Ethics application status
Approved
Date submitted
17/09/2012
Date registered
18/09/2012
Date last updated
17/09/2013
Type of registration
Retrospectively registered
Titles & IDs
Public title
Comparison of the efficacy and safety of adapalene versus benzoyl peroxide in the treatment of mild acne vulgaris; a clinical trial
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Scientific title
A randomized, double-blind, clinical trial to compare the efficacy (lesion number), side effects, and patient's satisfaction rate of topical adapalene and benzoyl peroxide in the cases with mild acne vulgaris
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Secondary ID [1]
281241
0
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:
Acne vulgaris
287433
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Condition category
Condition code
Skin
287769
287769
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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
Patients received topical adapalene 0.1% gel (ADA; Differin; Galderma, Watford, UK) once daily for 8 weeks.
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Intervention code [1]
285708
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Treatment: Drugs
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Comparator / control treatment
Patients received topical BPO 2.5% gel (Benzac AC; Galderma, Watford, UK) once daily for 8 weeks.
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Control group
Active
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Outcomes
Primary outcome [1]
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Number of facial acne lesions: For this purpose, the open and closed comedones (noninflammatory lesions), as well as the pustules, papules, and nodules (inflammatory lesions) were counted on the forehead, cheeks, nose, and chin by a single investigator under appropriate magnification.
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Assessment method [1]
287998
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Timepoint [1]
287998
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At the first, second and third months posttreatment
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Secondary outcome [1]
299233
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Side effects including facial redness, dryness, and peeling which were reported by an investigator after thorough physical exam; as well as facial itching and burning which were solicited from the patient.
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Assessment method [1]
299233
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Timepoint [1]
299233
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At the first, second and third months posttreatment
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Secondary outcome [2]
299266
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Patient?s overall satisfaction which was inquired and rated as poor, intermediate, good or excellent
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Assessment method [2]
299266
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Timepoint [2]
299266
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At the end of the third month posttreatment.
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Eligibility
Key inclusion criteria
Diagnosis of acne vulgaris
Mild disease according to the Evaluator Global Severity Score (grade 2)
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Minimum age
18
Years
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Maximum age
40
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
Severe acne vulgaris
Any dermatologic conditions requiring systemic therapy
Nursing/pregnant women
The women were planning for pregnancy
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled 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
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 4
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Type of endpoint/s
Safety/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
1/01/2011
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Actual
1/01/2011
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Date of last participant enrolment
Anticipated
6/04/2012
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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
60
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
4559
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Iran, Islamic Republic Of
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State/province [1]
4559
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Funding & Sponsors
Funding source category [1]
286020
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Self funded/Unfunded
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Name [1]
286020
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Dr Rohollah F Fouladi
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Address [1]
286020
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Azadi Ave., Hafe Square, Sina Hospital, Department of Dermatology, East Azerbayjan, Tabriz, PO BOX: 5163639888
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Country [1]
286020
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Iran, Islamic Republic Of
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Primary sponsor type
Individual
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Name
Dr Shahla Talghini
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Address
Azadi Ave., Hafe Square, Sina Hospital, Department of Dermatology, East Azerbayjan, Tabriz, PO BOX: 5163639888
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Country
Iran, Islamic Republic Of
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Secondary sponsor category [1]
284836
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Individual
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Name [1]
284836
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Dr Rohollah F Fouladi
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Address [1]
284836
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Azadi Ave., Hafe Square, Sina Hospital, Department of Dermatology, East Azerbayjan, Tabriz, PO BOX: 5163639888
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Country [1]
284836
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Iran, Islamic Republic Of
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Ethics approval
Ethics application status
Approved
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Summary
Brief summary
The present clinical trial aims to compare the efficacy and safety profile of topical adapalene 0.1% and BPO 2.5% gels in patients with mild acne vulgaris. For this purpose, 60 patients equally received either topical adapalene 0.1% gel or topical BPO 2.5% gel once daily to the entire face (except periocular area and lip) for two consecutive months. Three months later, number of lesions, side effects and patients' satisfaction were compared between the two groups.
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Trial website
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Trial related presentations / publications
Babaeinejad SH, Fouladi RF. The efficacy, safety and tolerability of adapalene versus benzoyl peroxide in the treatment of mild acne vulgaris; a randomized trial. J Drugs Dermatol. 2013 Sep 1;12(9):1033-8.
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Public notes
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Contacts
Principal investigator
Name
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Dr Rohollah Fadaei Fouladi
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Address
34719
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Azadi Ave., Hafe Square, Sina Hospital, Department of Dermatology, East Azerbayjan, Tabriz, PO BOX: 5163639888
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Country
34719
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Iran, Islamic Republic Of
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Phone
34719
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+989144122542
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Fax
34719
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Email
34719
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[email protected]
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Contact person for public queries
Name
17966
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Rohollah F Fouladi
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Address
17966
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Azadi Ave., Hafe Square, Sina Hospital, Department of Dermatology, East Azerbayjan, Tabriz, PO BOX: 5163639888
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Country
17966
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Iran, Islamic Republic Of
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Phone
17966
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+989144122542
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Fax
17966
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Email
17966
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[email protected]
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Contact person for scientific queries
Name
8894
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Rohollah F Fouladi
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Address
8894
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Azadi Ave., Hafe Square, Sina Hospital, Department of Dermatology, East Azerbayjan, Tabriz, PO BOX: 5163639888
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Country
8894
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Iran, Islamic Republic Of
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Phone
8894
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+989144122542
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Fax
8894
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Email
8894
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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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