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NCT04427904

Bupivacaine Versus Lidocaine Infiltration for Postoperative Pain in Thyroid Surgery

Status unknown Phase 2 Last updated 28 November 2023
What this trial tests

Phase 2 trial testing Bupivacaine 0.5% with 1:200 000 epinephrine in Postoperative Pain in 210 participants. Status unknown.

Timeline
1 June 2022
Primary endpoint
31 December 2024
31 December 2025

Quick facts

Lead sponsorSt. Joseph's Healthcare Hamilton
PhasePhase 2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment210
Start date1 June 2022
Primary completion31 December 2024
Estimated completion31 December 2025
Sites1 location across Canada

Drugs / interventions tested

Conditions studied

Sponsor

St. Joseph's Healthcare Hamilton — full company profile →

Who can join

Adults 18 to 100, any sex, with Postoperative Pain or Thyroid Diseases. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to compare the efficacy of Bupivicaine and Lidocaine for postoperative pain control in thyroid surgery.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Postoperative Pain

Currently open trials in the same condition.

Other St. Joseph's Healthcare Hamilton 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/NCT04427904.

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