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Actively Recruiting

Phase Not Applicable
Age: 18Years - 90Years
All Genders
ID07324499

Study Comparing Plasma Levels of Bupivacaine and Dexamethasone After Interscalene Nerve Block with Different Dexamethasone Methods

Led by Pontificia Universidad Catolica de Chile · Updated on 2026-08-12

40

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying the effects of dexamethasone when given either around the nerve perineurally or through the vein intravenously during a single-shot interscalene nerve block for shoulder surgery. The study focuses on comparing blood levels of the local anesthetic bupivacaine and dexamethasone to better understand their absorption and effects. This research is important because previous findings suggest perineural dexamethasone may safely extend pain relief, but its exact action and systemic absorption are not well known. Participants will receive 20 mL of 0.25% bupivacaine combined with 8 mg of dexamethasone administered either perineurally or intravenously. The study is randomized and double-blind, involving 40 patients undergoing shoulder surgery that requires a single-shot interscalene block. Blood samples will be taken multiple times after the block to measure plasma concentrations of bupivacaine and dexamethasone. The trial compares these levels between the two groups to assess pharmacokinetics and block effectiveness. During the study, participants will have venous blood samples collected at several time points up to four hours post-block, plus one sample at discharge. Researchers will evaluate the plasma levels of both enantiomers of bupivacaine and dexamethasone, block duration, and opioid use. The study is conducted under medical supervision with careful monitoring of participants responses and safety throughout the trial period.

CONDITIONS

Brief Title

Effect of Dexamethasone on Plasma Levels of Bupivacaine and Dexamethasone After a Single-injection Interscalene Nerve Block.

Who Can Participate

Age: 18Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • ASA I-II patients scheduled for shoulder surgery requiring a single-needle interscalene block
  • Body mass index (BMI) between 20 and 34 kg/m2
  • Age between 18 and 90 years
Not Eligible

You will not qualify if you...

  • Chronic opioid use
  • Liver failure
  • Kidney failure
  • Allergy to any drugs used in the study protocol

Research Team

A

Andrea Araneda, MD

R

Ricardo Fuentes, MD

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