Geneva, Nov. 2 -- International Clinical Trials Registry received information related to the study (ChiCTR2600135075) titled 'Effect of tegileridine for postoperative analgesia on quality of postoperative recovery in patients undergoing posterior lumbar decompression and fusion with internal fixation' on Oct. 23.
Study Type: Observational study
Study Design:
Cohort study
Primary Sponsor: Liuzhou Worker's Hospital
Condition:
Lumbar degenerative disease (undergoing posterior lumbar interbody fusion)
Intervention:
Sufentanil group:None
Recruitment Status: Not Recruiting
Phase: N/A
Date of First Enrollment: 2026-11-01
Target Sample Size: Sufentanil group:60;Tegileridine group:60;
Countries of Recruitment:
China
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