MedTrace Logo

Patient Satisfaction With Postoperative Follow up After Minimally Invasive Hysterectomy

NCT03642743 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 174

Last updated 2021-04-26

No results posted yet for this study

Summary

This prospective, randomized control trial will evaluate patient satisfaction with the number of postoperative follow up visits after minimally invasive hysterectomy for the treatment of non-cancerous conditions at an urban academic hospital in Louisville, Kentucky. Patients will be randomized to receive either a two and six week postoperative follow up visits versus a postoperative follow up visit at six weeks alone.

Conditions

  • Minimally Invasive Surgery
  • Hysterectomy
  • Postoperative
  • Satisfaction

Interventions

OTHER

postoperative follow up appointment

Comparison of two and six week postoperative follow up versus a six week postoperative follow up alone

Sponsors & Collaborators

  • University of Louisville

    lead OTHER

Principal Investigators

  • Shan Biscette, MD · University of Louisville School of Medicine

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-08-08
Primary Completion
2020-03-31
Completion
2020-03-31

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03642743 on ClinicalTrials.gov