Patient-Reported Outcome Measures and Satisfaction for Same-Day Discharge Following Robotic Hysterectomy

Overview

About this study

The purpose of this study is to measure patient-reported outcomes regarding symptoms, function, and patient satisfaction following a simple robotic hysterectomy, and compare these measures between patients who are discharged on the day of surgery and patients who stay overnight in the hospital.

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 women scheduled to undergo a robotic hysterectomy with or without bilateral salpingo-oophorectomy for benign indications.This will include patients who will have uterosacral ligament suspension at the time of hysterectomy, as this is part of routine hysterectomy at our institution, but will not include patients undergoing additional procedures for pelvic floor prolapse or incontinence.

Exclusion Criteria:

Non-English speakers
Patients with cognitive impairment hindering completion of the survey Patients undergoing emergency surgery

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
Scottsdale/Phoenix, Ariz. Mayo Clinic principal investigator Johnny Yi, M.D.	Closed for enrollment

Mayo Clinic Location

Status

Scottsdale/Phoenix, Ariz.

Mayo Clinic principal investigator

Johnny Yi, M.D.

Closed for enrollment

More information

Publications

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