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NCT03642743

Patient Satisfaction With Postoperative Follow up After Minimally Invasive Hysterectomy

Completed NA Last updated 26 April 2021
What this trial tests

NA trial testing postoperative follow up appointment in Minimally Invasive Surgery in 174 participants. Completed in 31 March 2020.

Timeline
8 August 2018
Primary endpoint
31 March 2020
31 March 2020

Quick facts

Lead sponsorUniversity of Louisville
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposehealth services research
Enrollment174
Start date8 August 2018
Primary completion31 March 2020
Estimated completion31 March 2020
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of Louisville

Who can join

Adults 18 to 70, female only, with Minimally Invasive Surgery or Hysterectomy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Minimally Invasive Surgery

Currently open trials in the same condition.

Other University of Louisville trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03642743.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing