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NCT05386732

Safety and Efficacy of the 4MD Micro Needling Device in the Treatment of Acne Scars

Completed Last updated 27 May 2022
What this trial tests

trial testing Micro needling in Acne Scarring in 22 participants. Completed in 9 October 2020.

Timeline
19 June 2020
Primary endpoint
9 October 2020
9 October 2020

Quick facts

Lead sponsorDermapenworld
StatusCompleted
Study typeOBSERVATIONAL
Enrollment22
Start date19 June 2020
Primary completion9 October 2020
Estimated completion9 October 2020
Sites1 location across Spain

Drugs / interventions tested

Conditions studied

Sponsor

Dermapenworld

Who can join

Adults 18 to 65, any sex, with Acne Scarring. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of this post market clinical follow-up study is to assess the safety and effectiveness of the 4MD microneedling device in reducing scarring of atrophic acne scars. The Primary endpoint was to show a reduction in acne scarring in accordance with the Acne Scar Assessment Scale as used by Skinpen (Bellus Medical (DEN160029)). Goodman and Baron and Jacob acne scar assessment and classification will also be utilized Safety endpoint: incidence of adverse events and side effects

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Trials testing the same drug.

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Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05386732.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing