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Randomized Study of Preoperative Dexamethasone for Quality of Recovery in VATS Lung Resection Patients

NCT02275702 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2021-08-25

No results posted yet for this study

Summary

The proposed study is a randomized, double-blind, placebo-controlled evaluation if a small dose of IV dexamethasone during induction anesthesia in association to pre and postoperative intercostal nerve block, improves quality of recovery of thoracoscopic lung resection patients.

Conditions

Interventions

DRUG

Dexamethasone IV

It will be administered at the induction of the anesthesia

DRUG

Saline solution

Sponsors & Collaborators

  • Laval University

    lead OTHER

Principal Investigators

  • Paula A. Ugalde, Medicin · Institut Universitaire de Cardilogie et Pneumologie de Québec, IUCPQ

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-10-31
Primary Completion
2016-10-31
Completion
2016-12-31

Countries

  • Canada

Study Locations

More Related Trials

Entities

Diseases

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 NCT02275702 on ClinicalTrials.gov