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Clinical Trials/NCT06801938
NCT06801938RecruitingNot Applicable

Comparison of Complications Detected by Perioperative Cystoscopy Combined With Methylene Blue Test and Postoperative Cystoscopy in TVT and TOT Operations

Gaziosmanpasa Research and Education Hospital1 site in 1 country58 target enrollmentStarted: January 1, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
58
Locations
1
Primary Endpoint
rate of complication detection

Study Overview

Brief Summary

Comparison of complications detected by perioperative cystoscopy combined with methylene blue test and postoperative cystoscopy in TVT and TOT operations.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 85 Years (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Providing consent to participate in the study
  • •Being between the ages of 18 and 85
  • •Having stress urinary incontinence
  • •No active cardiac disease
  • •No connective tissue disorders (e.g., Marfan syndrome)
  • •No known gynecological malignancy
  • •BMI under 30
  • •No chronic constipation
  • •No inflammatory bowel disease

Exclusion Criteria

  • •Not providing consent to participate in the study
  • •Being under 18 or over 85 years old
  • •Not having stress urinary incontinence
  • •Having active cardiac disease
  • •Having connective tissue disorders (e.g., Marfan syndrome)
  • •Having a known gynecological malignancy
  • •Having a BMI over 30
  • •Having chronic constipation
  • •Having inflammatory bowel disease

Arms & Interventions

Perioperative Methylene Blue and Cystoscopy with Postoperative Cystoscopy for Complication Detection

Experimental

This arm includes patients with stress urinary incontinence who will undergo perioperative methylene blue test and cystoscopy, followed by postoperative cystoscopy to detect any complications. The aim is to assess the ability of these methods to identify complications in the postoperative period.

Intervention: Perioperative Cystoscopy and Methylene Blue Test (Procedure)

Outcomes

Primary Outcomes

rate of complication detection

Time Frame: 6 months

Specifically, it would compare the ability of the perioperative methylene blue test and cystoscopy versus postoperative cystoscopy to detect complications. This measure will be used to evaluate the accuracy and effectiveness of both methods

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other Gov
Responsible Party
Sponsor

Study Sites (1)

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