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Emulsion 8-Week Anti-acne Efficacy Clinical Study

StatusActive, Not Recruiting
PhaseNot applicable
SponsorChinaNorm
Started
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Record History

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  1. Notable Primary endpoints revised (11)
    • Secondary endpoints: details revised at 1 of 1 entry
    v2
  2. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
15 trials monitored
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65 male and female adult subjects will be enrolled in the study, recruited according to inclusion and non-inclusion criteria listed below, at least 60 subjects should complete questionnaire, at least 40 of them should complete clinical assessment, instrumental measurement and image capture. 20 of them should complete lipid sample collection, and at least 30 of them should complete the RCM captured.
Trial Details
NCT Number NCT06985745
Lead Sponsor ChinaNorm
Conditions
(from sponsor)
Female, Male, Acne
Related terms Acne Vulgaris
Enrollment 66 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov