PRP Injections for Genitourinary Syndrome of Menopause

Description

Platelet-rich plasma (PRP) is autologous blood which has been centrifuged to separate the supernatant resulting in a solution with high concentration of platelets. Injection of PRP stimulates cell growth and can has been proven safe and effective for uses in orthopedics, dermatology, and gynecology. Despite the relative paucity of data, the use of PRP as a therapy for sexual dysfunction and genitourinary symptoms in the setting of menopause has been patented as the O-Shot and V-Shot. This is a single-blinded randomized control trial to determine if PRP injections into the anterior vaginal wall improve sexual functioning in women diagnosed with the genitourinary syndrome of menopause (GSM) characterized by vaginal dryness/irritation.

Conditions

PRP, Sexual Function Disturbances, Genitourinary Syndrome of Menopause, Postmenopausal Symptoms, Vaginal Atrophy

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Study Overview

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Study Details

Study overview

Platelet-rich plasma (PRP) is autologous blood which has been centrifuged to separate the supernatant resulting in a solution with high concentration of platelets. Injection of PRP stimulates cell growth and can has been proven safe and effective for uses in orthopedics, dermatology, and gynecology. Despite the relative paucity of data, the use of PRP as a therapy for sexual dysfunction and genitourinary symptoms in the setting of menopause has been patented as the O-Shot and V-Shot. This is a single-blinded randomized control trial to determine if PRP injections into the anterior vaginal wall improve sexual functioning in women diagnosed with the genitourinary syndrome of menopause (GSM) characterized by vaginal dryness/irritation.

Vaginal Injection of Platelet Rich Plasma (PRP) for the Genitourinary Syndrome of Menopause (GSM)

PRP Injections for Genitourinary Syndrome of Menopause

Condition
PRP
Intervention / Treatment

-

Contacts and Locations

Washington

MedStar Lafayette Medical Centre, Washington, District of Columbia, United States, 20036

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Women (assigned female at birth) at least 18 years old with a clinical diagnosis of GSM
  • * Sexually active with at least one episode of sexual activity per week in the preceding 4 weeks defined as follows: Partnered or solo penetrative or non-penetrative stimulation of the clitoris or vagina
  • * English-speaking
  • * Willingness and able to comply with the study requirements
  • * Symptomatic pelvic organ prolapse protruding beyond the hymen)
  • * History of prior vaginal mesh or midurethral mesh sling surgery
  • * History of pelvic radiation or genital tract malignancy
  • * Current symptomatic pelvic organ prolapse (stage II or greater)
  • * Active vulvar dermatoses or genitourinary infection
  • * Unable to hold anticoagulation
  • * Hormonal replacement therapy (systemic, local, or vaginal) within 3 months of participation
  • * Pregnancy or pre-menopausal status

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

Medstar Health Research Institute,

Study Record Dates

2024-12