Improving vagina laxity with a new formulation
Safety and Efficacy of Formulation Containing Stem Cell Secretome and Liquorice Root Extract for Improving Vagina Laxity of Women in Malaysia: A Pilot Study.
NA · Ungku Shahrin Medical Aesthetic Research & Innovation (USMARI) Centre · NCT05710536
This study is testing a new treatment made from natural ingredients to see if it can help women aged 40 to 55 improve vaginal tightness.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 18 (estimated) |
| Ages | 40 Years to 55 Years |
| Sex | Female |
| Sponsor | Ungku Shahrin Medical Aesthetic Research & Innovation (USMARI) Centre (industry) |
| Locations | 1 site (Petaling Jaya, Selangor) |
| Trial ID | NCT05710536 on ClinicalTrials.gov |
What this trial studies
This pilot study investigates the safety and efficacy of a formulation containing stem cell secretome and licorice root extract aimed at improving vagina laxity in Malaysian women aged 40 to 55. Over a duration of 5 weeks, participants will undergo assessments at baseline, week 2, and week 5 to evaluate changes in vagina laxity and monitor any adverse effects. The formulation is designed to stimulate cell rejuvenation and promote cell renewal through a blend of natural polypeptides and plant extracts.
Who should consider this trial
Good fit: Ideal candidates are Malaysian women aged 40 to 55 who are experiencing complaints of vagina laxity.
Not a fit: Patients who are pregnant, breastfeeding, or have undergone recent procedures for vagina laxity may not benefit from this study.
Why it matters
Potential benefit: If successful, this formulation could provide a non-invasive option for women experiencing vagina laxity, enhancing their quality of life.
How similar studies have performed: While this approach is novel, similar studies exploring the use of natural formulations for vaginal health have shown promising results.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Malaysian women ( age 40 to 55 years old) * Complaint of vagina laxity * Willingness to participate in the study Exclusion Criteria: * Pregnant and breastfeeding women * Doing any surgical or non-surgical procedures to improved vaginal laxity condition such as laser and radiofrequency before participating in the study that might affect the study outcome * Presence of illness or taking any medication that might impact the study outcome or participants well-being
Where this trial is running
Petaling Jaya, Selangor
- Ungku Shahrin Medical Aesthetic Research & Innovation (USMARI) Centre — Petaling Jaya, Selangor, Malaysia (RECRUITING)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Healthy, Vagina laxity