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Clinical trialNCT03036085UnknownPhase 2/PHASE3Interventional

Liposomal Bupivacaine for Pain Control Following Thoracic Surgery.

SponsorMassachusetts General HospitalEnrollment200Local Anesthetics Causing Adverse Effects in Therapeutic UseOpioid DependencePain, PostoperativeThoracic Diseases
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The aims of the study are to compare the effectiveness and postoperative outcomes of liposomal bupivacaine vs plain bupivacaine following video-assisted thoracoscopic surgery. The investigators' hypothesis is that liposomal bupivacaine will decrease the postoperative pain and will be associated with more favorable postoperative outcomes when compared to plain bupivacaine following video-assisted thoracoscopic surgery.

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

  • Harald Ott, MD

    Division of Thoracic Surgery, Massachusetts General Hospital

    Principal Investigator

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

No facility list is in our current data snapshot for this study. The registry record on ClinicalTrials.gov ↗ carries any published locations. Why? →

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Bupivacaine →Epinephrine →Liposomal bupivacaineNormal saline
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
28 Feb 2017
Primary completion
31 Dec 2017
Completion
31 Dec 2017
Last update posted
30 Jan 2017
Registered enrollment
200
Registry id
NCT03036085

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 4 Nov 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.