Clinical Trials Directory

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UnknownNCT05768607

Laparoscopic Extraperitoneal ( Modified) Burch Colposuspension

Evaluation of the Results of Laparoscopic Extraperitoneal ( Modified) Burch

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
90 (estimated)
Sponsor
Gaziosmanpasa Research and Education Hospital · Other Government
Sex
Female
Age
25 Years – 75 Years
Healthy volunteers
Accepted

Summary

Urinary incontinence is a very common problem in women and can be seen at any age. Laparoscopic burch operation has been shown to be an effective, convenient and safe method in women with stress incontinence. Laparoscopic Burch operation is less invasive because it is advantageous in terms of hospitalization time, blood loss, pain and recovery time, but the disadvantage is the procedure time. Modified extraperitoneal technique may be a good method for lowering the procedure time.

Detailed description

In the research; The pre- and postoperative urodynamics of patients who underwent laparoscopic extraperitoneal (modified) burch operation in the Gynecology and Obstetrics Clinic of Istanbul Health Sciences University Gaziosmanpasa Training and Research Hospital will be compared. Surgical outcomes together with complications will also be assessed. In addition, the QUALITY OF LIFE (SF36), which determines the quality of life of the patients related to the urinary system functions, and the UROGENITAL DISTRESS INVENTORY (UDI - 6), INCONTINENCE IMPACT QUESTIONNAIRE (IIQ-7) questionnaires that determine the effects of urinary incontinence, will be assessed preoperatively and postoperative 6 months of the patients.

Conditions

Interventions

TypeNameDescription
PROCEDUREQuality of Life QUESTIONNAIRE (SF36)Units of a scale of the patients will be compared pre and postoperatively by using SF36
PROCEDUREINCONTINENCE IMPACT QUESTIONNAIRE (IIQ-7)Units of a scale of the patients will be compared pre and postoperatively by using IIQ-7
PROCEDUREUROGENITAL DISTRESS INVENTORY (UDI - 6)Units of a scale of the patients will be compared pre and postoperatively by using UDI - 6

Timeline

Start date
2023-01-17
Primary completion
2023-07-17
Completion
2023-07-30
First posted
2023-03-14
Last updated
2023-06-05

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT05768607. Inclusion in this directory is not an endorsement.