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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03626298
Other study ID # PapulexPaper1
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date August 1, 2016
Est. completion date April 30, 2018

Study information

Verified date August 2018
Source Rumah Sakit Pusat Angkatan Darat Gatot Soebroto
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Acne vulgaris (AV) is a chronic inflammatory disease of the pilosebaceous unit that affects seborrheic areas such as the face, back and chest. AV is characterized by blackheads, papules, pustules nodes and cysts with sequelae of hyperpigmentation and scarring. It is one of the most common skin disorders treated by dermatologists. Acne vulgaris can be found at any age, although it is more frequent in teenagers and young adults. The prevalence of AV in a population of 11 to 30 years old is approximately 80%. Due to its involvement of the face, it is considered to be a cosmetic problem, thus bearing a psychosocial burden.


Recruitment information / eligibility

Status Completed
Enrollment 125
Est. completion date April 30, 2018
Est. primary completion date December 31, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 12 Years to 50 Years
Eligibility Inclusion Criteria:

- moderate acne vulgaris

- 12 and up to 50 years old,

- agreed to become research participants and has signed the informed consent.

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Adapalene
third-generation topical retinoid primarily used in the treatment of mild-moderate acne. It is effective against acne conditions where comedones are predominant.
Nicotinamide, ABA and Zinc PCA
combination of three non-antibiotic active ingredients of nicotinamide, anti-bacterial adhesive agent (ABA) and zinc, or abbreviated as ANAZ to be well-tolerated by patients with acne vulgaris
Placebos
Placebo cream. to resemble an active medication or therapy so that it functions as a control; this is to prevent the recipient(s) and/or others from knowing (with their consent) whether a treatment is active or inactive, as expectations about efficacy can influence results.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Rumah Sakit Pusat Angkatan Darat Gatot Soebroto

Outcome

Type Measure Description Time frame Safety issue
Primary inflammatory and non-inflammatory acne lesion reduction number analyzed using GLMM objective evaluation was based on photographs of participants from three angles per visit. The outcome of efficacy was measured from the percentage reduction of inflammatory and non-inflammatory lesions number and analyzed using the GLMM (General Linear mixed Model) 6 weeks
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