vaginal laxity
Conditions
Interventions
Case series:NA
Sponsors
Department of Gynecology and Obstetrics, the University of Hong Kong - Shenzhen Hospital
Eligibility
Sex/Gender
Female
Age
20 Years to 50 Years
Inclusion criteria
Inclusion criteria: 1: Vaginal capacity from 3 to 5 fingers;age range from 20 to 50; sexually active; seeking surgical intervention; no desire for future fertility 2: The patient gives informed consent and voluntarily participates in the study. 3: Sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1: Acute pelvic inflammatory disease; patients with depression; taking medications that affect sexual function (such as antidepressants, antihypertensives, sildenafil, etc.);smokers; pregnant women; husbands with sexual dysfunction; high-grade cervical intraepithelial neoplasia or positive high-risk HPV; patients with malignant tumors in the reproductive system; women with future fertility requirements; patients with surgical contraindications, such as severe internal diseases that are not suitable for surgery; non-Chinese speakers. 2: Patients currently participating in other clinical trials. 3: Patients requesting conservative treatment and refusing surgery.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| FSFI,Female Sexual Function Index;PHQ-9,Patient Health Questionnaire -9;GAD-7,Generalized Anxiety Disorder 7;IIEF-5,International Index of Erectile Function -5;PEDT,Premature Ejaculation Diagnostic Tool; | — |
Countries
China
Contacts
Public ContactYuzhen Wei
University of Hong Kong-Shenzhen Hospital
Outcome results
None listed