erve-sparing aorto-iliac reconstruction surgery; functional outcome and clinical feasibility.

Recruiting

• Conditions: Abdominal aortic aneurysm; distended abdominal bloodvessel; 10003184; 10002363

• Registration Number: NL-OMON40467
• Lead Sponsor: eids Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 120

Inclusion Criteria

Every adult patient able to give consent, indicated to undergo open aortoiliac reconstruction surgery, is eligible for inclusion.

Exclusion Criteria

Patients with prior aortoiliac, para-aortic surgery, retroperitoneal radiation therapy, and/or retroperitoneal surgery will not be included.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Study parameters:<br /><br><br /><br>Sexual, urogenital and gastrointestinal function pre-, and post aortoiliac<br /><br>reconstruction surgery.<br /><br><br /><br>Outcome:<br /><br><br /><br>Results of the following questionnaires<br /><br><br /><br>Men:<br /><br><br /><br>Ejaculation questionnaire (Waldinger)<br /><br>Cleveland Clinic Fecal Incontinence Score<br /><br>Pac-sym questionnaire (Constipation)<br /><br>IIEF (International Index of Erectile Dysfunction)<br /><br>ICIQ-Mluts (Male lower urinary tract symptoms)<br /><br><br /><br>Women:<br /><br><br /><br>FSDS (female sexual distress scale)<br /><br>Cleveland Clinic Fecal Incontinence Score<br /><br>Pac-sym questionnaire (Constipation)<br /><br>ICIQ-fluts (Female lower urinary tract symptoms)<br /><br>FSFI (Female sexual function index)</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Results of post-orgasmic urine analysis in men suffering from postoperative<br /><br>ejaculation disorders.<br /><br><br /><br>Results of the 'Feasibility' questionnaire for the surgeon.</p><br>