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Dexamethasone clinical trials

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NCT ID: NCT03874936 Completed - Postoperative Pain Clinical Trials

The Effect of Perioperative Dexamethasone Administration on Postoperative Pain in Patients Undergoing Periacetabular Osteotomy.

PAODEX
Start date: November 12, 2020
Phase: Phase 2/Phase 3
Study type: Interventional

This is an investigator-initiated, Danish mono-center, randomized, placebo-controlled, parallel group, double-blind, superiority trial of dexamethasone on postoperative pain management on patients undergoing operation for hip dysplasia with the periacetabular osteotomy procedure (PAO). 90 adults undergoing PAO will be enrolled. The primary outcome is to compare the effect of dexamethasone relative to placebo on cumulated postoperative morphine consumption at 48 hours. Key secondary outcomes include comparing the effect of repeated doses of dexamethasone relative to a single dose on cumulated postoperative morphine consumption at 48 hours, and to determine if dexamethasone is superior to placebo for: Perception of pain intensity, prevalence and degree of postoperative nausea and vomiting, and patient-reported outcome measures.

NCT ID: NCT03688269 Completed - Dexamethasone Clinical Trials

Minimal Effective Concentration (EC90) of Ropivacaine

AxiRopiDexa
Start date: October 5, 2018
Phase: Phase 3
Study type: Interventional

Prospective up and down sequential evaluation of the minimal effective concentration of perineural ropivacaine for 90% success in axillary brachial plexus block with the injection of intravenous dexamethasone or saline placebo during regional anesthesia performance

NCT ID: NCT03456752 Completed - Clinical trials for Inflammatory Bowel Diseases

Perioperative Dexamethasone on Postoperative Outcome in IBD

Start date: June 1, 2018
Phase: Phase 2
Study type: Interventional

The objective of this RCT is to determine the efficacy of a single preoperative dose of Dexamethasone for accelerating the recovery and reducing the incidence of postoperative complications in adult patients undergoing intestinal resection for inflammatory bowel disease.

NCT ID: NCT03125941 Completed - Breast Cancer Clinical Trials

High vs Low Dose Dexamethasone on Complications in the Immediate Postoperative Phase After Mastectomy

DEX-MAS
Start date: March 27, 2017
Phase: Phase 4
Study type: Interventional

The aim of this study is to investigate the effect of a single preoperative high-dose steroid injection on complications in the immediate postoperative phase after breast cancer surgery, with removal of the breast (mastectomy). Primary outcome is the proportion patients who require transfer to the post anaesthesia care unit (PACU) and the proportion that can be transferred directly to the ward. Secondary outcomes are organospecific complications in the postanesthesia phase, pain and nausea the first 5 days, seroma and wound infection the first 14 days and readmissions the first 30 days after surgery. The investigators hypothesize that the frequency of transfer to the PACU and organospecific complications will be lower among patients receiving high dose dexamethasone. The investigators hypothesize, that there will be no difference in wound infections, seroma or readmissions.