Trials / Completed
CompletedNCT05715489
Pectopexy Surgery Without Mesh
Evaluation of the Results of Laparoscopic Pectopexy Surgery Without Using Mesh
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 38 (actual)
- Sponsor
- Gaziosmanpasa Research and Education Hospital · Other Government
- Sex
- Female
- Age
- 30 Years – 75 Years
- Healthy volunteers
- Accepted
Summary
it is aimed to examine the effect of laparoscopic pectopexy surgery without mesh on Pelvic Organ Prolapse Measurement (POP-Q) and quality of life of the patient.
Detailed description
Every gynecological patient with prolapse is evaluated with POP-Q staging. The POP-Q staging to be performed before the laparoscopic pectopexy operation without mesh (performed by using non-melting sutures with natural tissue repair) performed on the patients will be compared with the POP-Q staging that will be performed 6 months after the operation. In addition, the quality of life of patients before and 6 months after the operation will be compared with the incontinence quality of life scale questionnaire of Pelvic Organ Prolapse / Incontinence Sexual Questionnaire (PISQ-12).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Comparison of pre and postoperative POP-Q values of the patients | Pectopexy Without Using Mesh will be applied to the patients and POP-Q values will be compared pre and postoperatively |
| PROCEDURE | Comparison of pre and postoperative PISQ-12 scores of the patients | Pectopexy Without Using Mesh will be applied to the patients and PISQ-12 scores will be compared pre and postoperatively |
Timeline
- Start date
- 2022-05-11
- Primary completion
- 2024-05-11
- Completion
- 2024-05-11
- First posted
- 2023-02-08
- Last updated
- 2024-10-01
Locations
1 site across 1 country: Turkey (Türkiye)
Source: ClinicalTrials.gov record NCT05715489. Inclusion in this directory is not an endorsement.