At a glance
ClinicalIndex Comparison RecordN/ACompleted· 68 enrolled
Drug / intervention
Not used remifentanil infusiondrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
The Effect of Remifentanil on Rebound Pain in Patients Receiving General Anesthesia for Shoulder Arthroplasty After Brachial Plexus Block for Postoperative Pain Control
In Brief
A clinical study evaluating Not used remifentanil infusion for Pain, Postoperative. Completed, enrolled 68 participants across 1 site.
Detailed Summary
The investigators will evaluate the influence of intraoperative remifentanil infusion on the postoperative hyperalgesia in patients receiving rotator cuff repair after brachial plexus block for postoperative analgesia.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPain, Postoperative
CountriesSouth Korea
Collaborators--
Timeline
N/ACompletedFinished
2020202120222023202420252026
First PostedJan 2020
Enrollment StartFeb 2020
Primary CompletionAug 2020
Study CompletionJan 2021
TodayJul 2026
First PostedJan 22, 2020
Enrollment StartFeb 14, 2020
Primary CompletionAug 12, 2020
Study CompletionJan 7, 2021
TodayJul 1, 2026
Enrollment to primary: 6 monthsPosted 6.4 years ago
Interventions
Not used remifentanil infusiondrug
Remifentanil is not used during operation