Same Day Discharge Following Pelvic Reconstructive Surgery

TriHealth Inc.54 enrolled

Overview

This is a prospective cross-sectional study in which patients undergoing major pelvic reconstructive surgery with total vaginal hysterectomy will be recruited and enrolled. At approximately 2 weeks and 12 weeks postoperatively, enrolled patients will be asked to complete a survey detailing their experience with SDD, surgical recovery, and advice for prospective patients.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Same Day Discharge Pelvic Organ Prolapse Total Vaginal Hysterectomy

Interventions

Pelvic Reconstructive SurgeryPROCEDURE

Pelvic Reconstructive Surgery including total vaginal hysterectomy

Eligibility

Sex: FEMALEMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Total vaginal hysterectomy with or without bilateral salpingectomy/oophorectomy * Apical repair with uterosacral ligament suspension or sacrospinous ligament fixation * They may also have any of the following concurrent procedures: Anterior repair, Posterior repair, Enterocele repair, Suburethral sling for incontinence * Surgery by one of the fellowship trained urogynecologists at TriHealth * English speaking Exclusion Criteria: * Enrollment in the "Diazepam Research Study" (Protocol ID:19-130) * Concomitant procedure with another surgeon * Chronic pain conditions that require daily use of narcotic pain medications (including but not limited to: chronic back or pelvic pain, interstitial cystitis, fibromyalgia) * Concomitant anal sphincteroplasty, mesh removal or use of mesh for prolapse (excluding sling procedures)

Locations (1)

Cincinnati Urogynecology Associates

Cincinnati, Ohio, United States

Outcomes

Primary Outcomes

Number of subjects who satisfied with the results of the surgery

Number of subjects who answered either "Very Satisfied" or "Satisfied" to a Likert scale question "How satisfied are you with the results of your surgery." The liker scale choices are "Very Satisfied", "Satisfied", "Neutral", "Unsatisfied", and "Very Unsatisfied."

Time frame: Approximately 2 weeks postoperatively

Secondary Outcomes

Number of subjects who satisfied with the results of the surgery

Time frame: Approximately 12 weeks postoperatively

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.