Pelvic organ prolapse
Conditions
Interventions
Experimental group :single-port laparoscopic lateral mesh suspension with improved micro puncture
Control group:Laparoscopic lateral suspension
Sponsors
Chengdu First People's Hospital
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1.Patients diagnosed with Pelvic Organ Prolapse Quantification (POP-Q) stage II or above who voluntarily opt for surgical treatment; 2.Patients who have not undergone previous surgery for pelvic organ prolapse or major pelvic surgery; 3.Patients with no significant surgical contraindications who can tolerate anesthesia and surgery; 4.Patients and their families have been informed about the study and agree to participate; 5.Patients who are able to comply with medical advice and avoid immediate strenuous physical activities postoperatively that may affect recovery.
Exclusion criteria
Exclusion criteria: 1.Patients with severe comorbidities; 2.Patients who had received hormone replacement therapy prior to enrollment; 3.Patients with concomitant severe pathologies of the uterus or ovaries, etc.; 4.Patients who underwent additional concurrent surgical procedures; 5.Patients in poor general condition unable to tolerate general anesthesia and surgery; 6.Patients unable to cooperate with or complete the follow-up.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The stage of Pelvic Organ Prolapse Quantification System; | — |
Secondary
| Measure | Time frame |
|---|---|
| The score of Pelvic Floor Distress Inventory-20;The score of Pelvic Floor Impact Questionnaire-7;the score of Pelvic Organ Prolapse/Urinary Incontinence Sexual Function Questionnaire; | — |
Countries
China
Contacts
Public ContactLi Min
Chengdu First People's Hospital
Outcome results
None listed