Clinical Trials Directory

Trials / Terminated

TerminatedNCT05710536

Safety and Efficacy of Formulation for Improving Vagina Laxity: A Pilot Study

Safety and Efficacy of Formulation Containing Stem Cell Secretome and Liquorice Root Extract for Improving Vagina Laxity of Women in Malaysia: A Pilot Study.

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
18 (actual)
Sponsor
USMARI Research & Innovation Centre · Industry
Sex
Female
Age
40 Years – 55 Years
Healthy volunteers
Accepted

Summary

This study is conducted to investigate the safety and efficacy of the formulation containing stem cell secretome and licorice root extract in improving vagina laxity (VL) condition of women in Malaysia. This formulation may stimulate cell rejuvenation and trigger cell renewal efficiently as they contained rich mixture of natural, bioavailable polypeptides and plant extracts and these might help improving the VL condition in women. The study duration is 5 weeks and vagina assessment will be carried out at baseline, week 2 and week 5.The main objectives of this study are: 1. To assess the vagina laxity of women in Malaysia after using the formulation. 2. To observe any adverse effect occurrence with the use of the formulation.

Conditions

Interventions

TypeNameDescription
OTHERFormulation XThis formulation containing stem cell secretome and liquorice root extract

Timeline

Start date
2023-12-01
Primary completion
2024-10-31
Completion
2024-12-30
First posted
2023-02-02
Last updated
2026-03-06

Locations

1 site across 1 country: Malaysia

Source: ClinicalTrials.gov record NCT05710536. Inclusion in this directory is not an endorsement.