Skip to content

Effect of Platelet-Rich Plasma (PRP) on Vaginal Maturation Index in Postmenopausal Women with Genitourinary Syndrome of Menopause: A Prospective Cohort Study

Effect of Platelet-Rich Plasma (PRP) on Vaginal Maturation Index in Postmenopausal Women with Genitourinary Syndrome of Menopause: A Prospective Cohort Study

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250717001
Enrollment
27
Registered
2025-07-17
Start date
2025-07-25
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Genitourinary Syndrome of Menopause Genitourinary syndrome of Menopause (GSM), Autologous PRP, Vaginal Maturation index

Interventions

The PRP (Platelet-Rich Plasma) product is derived from the patient herself. A blood sample of 10 ml is drawn and collected in a clotted blood tube. The sample is then centrifuged using a double centri
Experimental Biological/Vaccine

Sponsors

Research Fund, Faculty of Medicine, Thammasat University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Postmenopausal women aged between 45 and 70 years 2. Diagnosed with Genitourinary Syndrome of Menopause (GSM) based on clinical symptoms (vaginal dryness, dyspareunia) 3. Low baseline Vaginal Maturation Index (VMI) (less than 50% superficial and intermediate cells) 4. Willing and able to provide informed consent through a comprehensive informed consent process

Exclusion criteria

Exclusion criteria: 1. Currently using estrogen in any form 2. History of radiation therapy or pelvic surgery affecting the urinary or reproductive systems 3. Present genital or urinary tract infection 4. Abnormal bleeding or platelet disorders 5. Contraindications to blood draw or injection

Design outcomes

Primary

MeasureTime frame
Vaginal maturation index time of intervention, 1 month and 3 months after intervention use VMI scoring formula

Secondary

MeasureTime frame
Visual analog scale time of intervention, 1 month and 3 months post-intervention according to scale description ,Vulvovaginal symptoms questionnaire time of intervention, 1 month and 3 months post-intervention questionnaire interview ,Safety time of intervention, 1 month and 3 months post-invention adverse effects report,Feasibility After end of the intervention Retention rate and dropout rate

Countries

Thailand

Contacts

Public ContactTewit Siridet

Thammasat university

ballskas@hotmail.com0862888088

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026