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NCT04118777

Postoperative Narcotic Use After Laparoscopic Gynecologic Surgery

Withdrawn NA Last updated 20 July 2021
What this trial tests

NA trial testing Ropivacaine in Pelvic Pain. Withdrawn.

Timeline
1 May 2020
Primary endpoint
30 June 2020
30 July 2020

Quick facts

Lead sponsorUniversity of Tennessee, Chattanooga
PhaseNA
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Start date1 May 2020
Primary completion30 June 2020
Estimated completion30 July 2020

Drugs / interventions tested

Conditions studied

Sponsor

University of Tennessee, Chattanooga

Who can join

Adults 18 to 65, female only, with Pelvic Pain or Endometriosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This will be a prospective, randomized, double blinded placebo-controlled study at Erlanger hospital. Eligible patients who provide consent will be randomized into one of two arms receiving continuous intra-peritoneal local anesthetic with 0.2% Ropivacaine or saline.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Ropivacaine

Trials testing the same drug.

Other recruiting trials for Pelvic Pain

Currently open trials in the same condition.

Other University of Tennessee, Chattanooga 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/NCT04118777.

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