Transgender Post-reassignment Urogynecologic Measures and Perceptions

Sexual Dysfunction Clinical Trial

Official title: Assessment of Postoperative Urologic and Pelvic Floor Complaints in Male-to-female Transgender Patients: a Mixed Methods Study

Status Recruiting

Clinical Trial Summary

The intent of this mixed methods study for transgender women after gender confirmation surgery is to characterize and subsequently create a validated screening questionnaire for postoperative urologic and pelvic floor symptoms. For individuals who seek gender-confirming treatment, about 13% undergo genital surgery for cosmetic purposes with or without gonadectomy, and this number is increasing. Patient satisfaction following surgery is high, particularly regarding sexual and cosmetic outcomes; however, unexpected negative functional outcomes such as bowel and bladder dysfunction and pelvic organ prolapse impact overall patient satisfaction. The available information suggests that 16-33% of patients experience incontinence postoperatively, with stress predominance, 32-47% experience abnormal voiding, and 24-66% experience overactive bladder symptoms. Outside of the typically assessed voiding symptoms, unique complaints of MTF postoperative patients include obstructive voiding symptoms due to urethral stenosis, persistent perimeatal erectile tissue, prostatic hypertrophy, and irritation from neovaginal tissue. Additionally, may of these patients develop symptomatic neovaginal prolapse, requiring re-suspension. We suggest that further clarification regarding MTF postoperative urologic and pelvic floor complaints can be achieved via a mixed methods approach. By using focus group interviews to create specific evaluative questions for this unique population, we can then prospectively assess patients undergoing surgery via a national multicenter sampling strategy. The goal of the study is to better understand the unique symptoms these women experience and create a validated, reliable screening questionnaire to monitor patients after surgery.

Clinical Trial Description

n/a

Related Conditions & MeSH terms

• Disease
• Gender Dysphoria
• Gender Identity Disorder of Adult
• Sexual Dysfunction
• Voiding Disorders

• NCT number: NCT03293771
• Study type: Observational [Patient Registry]
• Source: Weill Medical College of Cornell University
• Contact: Sarah Huber, MD
• Phone: 212-746-5352
• Email: sah2757@med.cornell.edu
• Status: Recruiting
• Start date: December 27, 2017
• Completion date: December 31, 2019