Trials / Unknown
UnknownNCT05888194
The Effect of Mucogyne® Gel on Wound Healing
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 118 (estimated)
- Sponsor
- Biocodex · Industry
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The aim of this post-market clinical follow up study is to confirm the efficacy and safety of topical application of Mucogyne® gel in the process of wound healing, when used in accordance with its approved labeling, in the context of postpartum perineal wounds.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Mucogyne® gel | In Mucogyne group, each eligible patient will receive a box of Mucogyne® gel. The patient will apply Mucogyne® gel, 48-hours after delivery, everyday, twice a day, massaging it into the intimate area, for a 10-day period. |
Timeline
- Start date
- 2023-06-12
- Primary completion
- 2024-05-01
- Completion
- 2024-05-01
- First posted
- 2023-06-05
- Last updated
- 2024-03-12
Locations
3 sites across 1 country: France
Source: ClinicalTrials.gov record NCT05888194. Inclusion in this directory is not an endorsement.