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Efficacy of Local Anesthetic Through Continuous Infusion

NCT04173312 · Status: UNKNOWN · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2022-02-23

No results posted yet for this study

Summary

Efficacy of using continuous infusion of local anesthetic for post operative pain control following laparotomy.

Conditions

  • Pain Control

Interventions

COMBINATION_PRODUCT

Bupivacaine infusion

Local systemic Infusion of anesthetic

COMBINATION_PRODUCT

Saline

Local systemic infusion of saline

Sponsors & Collaborators

  • Ascension Health

    lead INDUSTRY

Principal Investigators

  • Tarik Wasfie, MD · Ascension Health

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-01-04
Primary Completion
2023-01-31
Completion
2023-12-31
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04173312 on ClinicalTrials.gov