Geneva, Nov. 2 -- International Clinical Trials Registry received information related to the study (ChiCTR2600134884) titled 'Effect of Subanesthetic-Dose Esketamine on Postoperative Sleep Quality in Patients Undergoing Arthroscopic Rotator Cuff Surgery' on Oct. 21.
Study Type: Interventional study
Study Design:
Parallel
Primary Sponsor: Taizhou People's Hospital
Condition:
None
Intervention:
Esketamine group:Esketamine: 0.2 mg/kg intravenous bolus + continuous intraoperative infusion at 0.02 mg/kg/h.
Recruitment Status: Not Recruiting
Phase: N/A
Date of First Enrollment: 2026-10-21
Target Sample Size: Esketamine group:44;The normal saline group:44;
Countries of Recruitment:
China
To know more, visit https://www.chictr.o...