A Study to Assess the Effect of Pudendal Nerve Block for Postoperative Pain Control in Patients Undergoing Neo-vaginoplasty Procedure
Overview
Tab Title Description
Study type
InterventionalDescribes the nature of a clinical study. Types include:
- Observational study — observes people and measures outcomes without affecting results.
- Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
- Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
Study IDs
Site IRB
- Rochester, Minnesota: 17-008021
Sponsor Protocol Number: 17-008021
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:
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