None listed
Conditions
Brief summary
Platelet Rich Plasma (PRP) has been demonstrated to be effective and without serious side effects in multiple studies in the areas of wound care, orthopaedics, dental surgery and in a variety of cosmetic procedures. PRP activates pluripotent stem cells in the area of injection resulting in rejuvenation and even enhancement of damaged or undamaged tissue. The aqueous nature of PRP allows injection through a small bore needle and an even distribution throughout the tissue surrounding the injection site. women who presented with complaints of dyspareunia or other symptoms related to sexual dysfunction will be offered PRP injections into the periurethral area of the Skene's glands, vaginal wall and the clitoris and will be observed for their responses to this treatment. It will offer a cheap, easy, non-invasive and safe treatment for females with sexual dysfunction.
Interventions
A small sample of blood (5ml) is withdrawn from the patient, then spun in a centrifuge to separate the blood into layers. The platelet-rich plasma layer is carefully extracted, then injected back into the anterior and posterior vaginal wall, G-spot and clitoris. the procedure will take about 10 minutes after local anaesthetic cream application.procedure will be done in the outpatient clinic by gynaecology specialist with minimum 3 years experience.patients will receive four times injections 2wee
A small sample of blood (5ml) is withdrawn from the patient, then spun in a centrifuge to separate the blood into layers. The platelet-rich plasma layer is carefully extracted, then injected back into the anterior and posterior vaginal wall, G-spot and clitoris. the procedure will take about 10 minutes after local anaesthetic cream application.procedure will be done in the outpatient clinic by gynaecology specialist with minimum 3 years experience.patients will receive four times injections 2weeks a part.they will be evaluated by FSFI questionnaire after 2 months.
Sponsors
DOAA MOHAMED SALEH
Study design
Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Healthy volunteers
Yes
Inclusion criteria
sexually active females 18-60 years complaining of sexual dysfunction.
Exclusion criteria
1- psychological or mental illness. 2- male partner erectile dysfunction. 3- diabetic patients
Outcome results
None listed