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Same Day Discharge Following Pelvic Reconstructive Surgery

Patient's Perceptions Regarding Same Day Discharge Following Pelvic Reconstructive Surgery: What do They Want Other Patients to Know?

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04804826
Enrollment
54
Registered
2021-03-18
Start date
2021-06-14
Completion date
2022-04-06
Last updated
2024-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pelvic Organ Prolapse, Same Day Discharge, Total Vaginal Hysterectomy

Brief summary

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.

Interventions

Pelvic Reconstructive Surgery including total vaginal hysterectomy

Sponsors

TriHealth Inc.
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

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)

Design outcomes

Primary

MeasureTime frameDescription
Number of subjects who satisfied with the results of the surgeryApproximately 2 weeks postoperativelyNumber 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.

Secondary

MeasureTime frameDescription
Number of subjects who satisfied with the results of the surgeryApproximately 12 weeks postoperativelyNumber 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.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026