Vaginal invagination:defintion, clinical presentation and surgical management

Not Applicable

Recruiting

• Conditions: the presentation of vaginal invagination intraoperatively and postoperatively.; Surgery - Other surgery; Renal and Urogenital - Other renal and urogenital disorders

• Registration Number: ACTRN12611000014954
• Lead Sponsor: Dr. Corina Schmid

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2011-01-06
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 20

Inclusion Criteria

Women undergoing vaginal prolapse surgery with a intraoperative detected vaginal invagination will be included in this observational study.

Exclusion Criteria

This is only an observational study to describe the condition of vaginal invagination. All women will be asked postoperatively to participated for an audit. Patients can withdraw from the study at any time.

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Description and clinical presentation of vaginal invagination in women undergoing vaginal prolapse surgery[A vaginal invagination can only be detected intraoperatively.<br>An audit will be held as routinely performed in women undergoing prolapse surgery 6 weeks postoperatively.]

Secondary Outcome Measures

Name	Time	Method
Assessment of the outcome of the surgical intervention. Patients will be examined according to the ICS POP-Q system (tool to assess the pelvic floor) and patient will be asked to complete the Queensland Pelvic Floor Questionnaire before and after surgery. All patients undergoing pelvic floor surgery are asked to complete this questionnaire and are examined accoriding to the ICS POP-Q system.[baseline (intraoperatively) and 6 weeks postoperatively.]