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Evaluation of Patient Satisfaction With Blephaderm as a Complementary Care in Post-eyelid Surgery

StatusRecruiting
PhaseNot specified
Started
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Record History

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  1. Trial status: Not Yet Recruiting to Recruitingv2 Show 4 more changesShow less
    • Primary and study completion dates: May 15, 2026 to Dec 15, 2026
    • Start date changed from estimate of Nov 15, 2025 to Oct 30, 2025
    • Site details revised
    • Study title revised
  2. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
The goal of this non-interventional, open and monocentric study is to evaluate the satisfaction of 30 patients, after 3 months with Blephaderm eyelid cream, as a complementary care in post-eyelid surgery (Blepharopasty or ptosis). The participant will be asked to use Blephaderm twice a day. The patient satisfaction will be evaluated using a VAS scale.
Trial Details
NCT Number NCT07234292
Lead Sponsor Laboratoires Thea
Conditions
(from sponsor)		 Eyelid; Wound
Related terms Wounds and Injuries
Enrollment 30 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov