RecruitingNot Applicable

Comparison of Postoperative Quality of Recovery by Anesthetic Method in Patients Undergoing Shoulder Arthroscopy

South Korea140 participantsStarted 2024-10-30

Plain-language summary

The aim of this study is to compare the quality of recovery in patients undergoing arthroscopic shoulder surgery depending on the type of anesthesia used: 1. general anesthesia with preoperative brachial plexus block for intra- and postoperative analgesia 2. regional anesthesia (brachial plexus block) with intraoperative sedation.

Who can participate

Age range19 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients of age 19 years and above, scheduled for shoulder arthroscopic surgery Exclusion Criteria: * emergency operation * inflammation or infection at the site of nerve block administration * inability to perform the quality of recovery questionnaire due to dementia or delirium * severe lung disease (e.g. chronic obstructive pulmonary disease or interstitial lung disease) * contraindication to brachial plexus block * history of hypersensitivity or side effect to ropivacaine

What they're measuring

Quality of recovery (QoR-15) at 48 hours post-surgery

Timeframe: at 48 hours post-surgery

Trial details

NCT IDNCT06638112

SponsorSeoul National University Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-10-10

Contact for this trial

Hansol Kim, MD

+82220722467 hansolfrkr@gmail.com

View on ClinicalTrials.gov More Shoulder Arthroscopy trials