RecruitingNot ApplicableNCT07544667

Poly-L-Lactic Acid for Vulvovaginal Tissue Regeneration

Intravaginal Injection of Poly-L-Lactic Acid for Treatment of Cystocele: A Randomized Trial


Sponsor

Cassandra Kisby

Enrollment

20 participants

Start Date

May 1, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

Pelvic organ prolapse (POP) is a condition characterized by descent of vaginal walls, uterus and cervix, or the perineum and causes a sensation of vaginal bulge and pelvic pressure. Millions of women in the United States are affected, and the number is expected to rise significantly in the coming decades. Current treatments either involve conservative measures or surgery. Surgery may lead to changes in vaginal topography and scar tissue, both of which impact sexual function. There are no treatment options that restore vaginal tissue strength and preserve, even optimize, sensation and blood flow to the vagina. This project will evaluate the use of poly-L-lactic acid (PLLA), an FDA-approved biostimulant for dermatologic use with an expansive safety profile over the past decade, in the treatment of anterior wall POP and its impact on sexual function. Our study will compare intravaginal injection of PLLA vs. placebo in women with stage 2 cystocele and investigate safety and preliminary efficacy of PLLA. Prior study of regenerative biologics for the vulva and vagina have shown great promise, but use of these has not been explored for POP. This randomized controlled trial has the potential to shift the paradigm of prolapse management from surgical reconstruction to regeneration. This shift will prevent the risks of surgery and has the potential to improve sexual function and quality of life by resolving POP.


Eligibility

Sex: FEMALEMin Age: 21 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Placebo injection (sterile water) and a medical device called Poly-L-Lactic Acid (Sculptra) injection for people with cystocele, pelvic floor disorder, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 21 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEPoly-L-Lactic Acid (Sculptra) injection

Sculptra will be diluted in 8mL of sterile water and 1mL of lidocaine and injected across the anterior/ventral vagina

OTHERPlacebo injection (sterile water)

8mL of sterile water will be combine with 1mL of lidocaine for injection in the anterior/ventral vagina


Locations(1)

Duke Urogynecology, Patterson Place

Durham, North Carolina, United States

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NCT07544667


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