A Study to Assess the Effect of Pudendal Nerve Block for Postoperative Pain Control in Patients Undergoing Neo-vaginoplasty Procedure

Overview

About this study

The purpose of this study is to assess postoperative pain in patients who received pudendal block with quantitative outcomes charted in medical records such as total amount of analgesics received, intraoperative vitals, number of days till mobile, and patient reported pain scale.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Adult males (18 or older) underwent genital part of the gender confirmation surgery, and trans-females after the surgery.

Exclusion Criteria:

  • Cis-females, trans-males

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

Oscar Manrique, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

Study Results Summary

Not yet available

Supplemental Study Information

Not yet available

Additional contact information

Non-cancer trials contact form

Phone: 800-664-4542 (toll-free)

International patient clinical studies questions