BURCH Colposuspension or Transobturatuar Tape (TOT)

Incontinence Clinical Trial

Official title:

Which Anti-İncontinence Surgery Option is Better in Patients With Total Laparoscopic Hysterectomy? BURCH Colposuspension or Transobturatuar Tape (TOT)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03938844
• Other study ID #: 2018.01.07
• Status: Completed
• Start date: January 1, 2014
• Est. completion date: January 1, 2017

Study information

• Verified date: May 2019
• Source: Kanuni Sultan Suleyman Training and Research Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Stress urinary incontinence surgery combined with hysterectomy can often be applied to patients in the same session. The aim of this study was to determine which urinary incontinence surgery would be a better option for patients who would have hysterectomy.

The aim of this study was to retrospectively review the data of 69 patients between the ages of 2014 and 2017 who underwent total laparoscopic hysterectomy and anti-incontinence surgery (TOT and Burch) for benign indications (uterine pathology) and stress urinary incontinence (SUI). In addition to demographic data and preoperative examination findings, operative times, postoperative hemogram values, postvoiding residual amounts and complications were examined.

In addition, FSI test results of women with sexual activity were compared with ICIQ-UI and UDI-6 interrogations related to urinary incontinence.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 69
• Est. completion date: January 1, 2017
• Est. primary completion date: January 1, 2017
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 40 Years to 65 Years

Eligibility

Inclusion Criteria:

• tlh operation with benign reasons and planned,

• concurrent stress describing urinary incontinence,

• Women between the ages of 40-65

Exclusion Criteria:

• planned operation with malignant causes,

• urinary tract infection,

• medication area for incontinence

Related Conditions & MeSH terms

• Incontinence

Intervention

Procedure:
• BURCH Colposuspension
stress urinary incontinence surgery ( burch or tot)
• TOT

Locations

Country	Name	City	State
Turkey	Kanuni Sultan Süleyman Training and Research Hospital	Istanbul

Sponsors (1)

Lead Sponsor	Collaborator
Kanuni Sultan Suleyman Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	operation time	The duration of the procedure for stress urinary incontinence surgery was evaluated. recorded in minutes.	2 years
Primary	postoperative hemogram values	postoperative hemogram values were evaluated. Recorded in g / dl.	2 years
Primary	postvoiding residues	postvoiding residues were measured. Recorded in ml.	2 years