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NCT02257346

Intravenous Lidocaine and Quality of Recovery After Cesarean Delivery

Withdrawn NA Last updated 9 June 2022
What this trial tests

NA trial testing Lidocaine in Pregnancy. Withdrawn.

Timeline
1 November 2014
Primary endpoint
15 February 2015
15 February 2015

Quick facts

Lead sponsorNorthwestern University
PhaseNA
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Start date1 November 2014
Primary completion15 February 2015
Estimated completion15 February 2015
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Northwestern University

Who can join

18 and older, female only, with Pregnancy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

When given intravenously, the local anesthetic lidocaine has been shown to decrease the amount of pain medication patients require when recovering from several types of surgeries. Cesarean delivery is a very common surgery in the United States, effecting more than 1 million women each year. The investigators hypothesize that lidocaine, given during and immediately after a patient undergoes a cesarean section, will help improve a mother's overall recovery experience, as well as positively influence bonding with her new baby.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Continuous intravenous perioperative lidocaine infusion for postoperative pain and recovery in adults.
    Weibel S, Jelting Y, Pace NL, Helf A, et al · · 2018 · cited 188× · PMID 29864216 · DOI 10.1002/14651858.cd009642.pub3

Verify or expand the search:

Other trials of Lidocaine

Trials testing the same drug.

Other recruiting trials for Pregnancy

Currently open trials in the same condition.

Other Northwestern University 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/NCT02257346.

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