Evaluation of Patient Satisfaction With Blephaderm as a Complementary Care in Post-eyelid Surgery
ConditionEyelid; Wound
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorLaboratoires Thea
About this trial
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.
Eligibility criteria
Qualifiers
Age ≥ 18 years old
Patients planning a blepharoplasty or a ptosis surgery in at least one eye.
Patient affiliated to a health social security system
Female of childbearing potential should use a medically accepted contraceptive regimen since at least 12 weeks before the beginning of the study, during all the study and at least 1 month after the study end.
Disqualifiers
Pregnant or nursing woman or planning a pregnancy during the study.
Patient who had been deprived of their freedom by administrative or legal decision
Minor patient.
Major patient who is under guardianship or who is not able to express his non opposition.
Trial design
Treatments tested in this trial
- Cosmetic: Blephaderm
Treatment groups
30 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov