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NOT YET RECRUITING
NCT07313553
NA

Prevention of Rebound Pain After Axillary Block

Sponsor: University Tunis El Manar

View on ClinicalTrials.gov

Summary

This will be a single-center randomized double blind placebo control clinical trial. In the cohort of patients undergoing hand surgery under axillary nerve block, participants are recruited from those who are willing to consent and participate in the study, and will be randomly 1:1 divided into intervention group and placebo group.

Official title: The Effect of Perineural Dexamethasone on Preventing Rebound Pain After Axillary Plexus Block in Hand Surgery

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2026-01-12

Completion Date

2026-09-30

Last Updated

2026-01-02

Healthy Volunteers

No

Interventions

OTHER

Saline

2 ml saline solution are added to 30 ml of a 50/50 mixture of isobaric bupivacaine 0.5% and lidocaine 1%

DRUG

Dexamathsone 4mg/ml associated with experimental arm

Intervention group will receive 30 ml of a 50/50 mixture of isobaric bupivacaine 0.5% and lidocaine 1%, containing 8 mg of dexamethasone.