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NCT03906617

Bupivacaine/Epinephrine +Dexamethasone vs. Liposomal Bupivacaine

Recruiting now Phase 4 Last updated 12 November 2021
What this trial tests

Phase 4 trial testing Intercostal nerve block and wound infiltration with liposomal bupivacaine in Robotic Lung Surgery in 34 participants. Currently enrolling.

Timeline
10 April 2019
Primary endpoint
10 April 2022
10 June 2022

Quick facts

Lead sponsorThe Cooper Health System
PhasePhase 4
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment34
Start date10 April 2019
Primary completion10 April 2022
Estimated completion10 June 2022
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

The Cooper Health System — full company profile →

Who can join

Adults 18 to 90, any sex, with Robotic Lung Surgery. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will assess analgesia after robotic lung surgery. Subjects will be randomized to receive wound infiltration and intercostal nerve block with either liposomal bupivacaine or bupivacaine/epinephrine + dexamethasone. Liposomal bupivacaine is a newer local anesthetic product and has not been compared to a combination of bupivacaine/epinephrine + dexamethasone in the context of pain control after robotic lung surgery.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other The Cooper Health System trials

Trials by the same sponsor.

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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/NCT03906617.

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