Clinical Trial

Oliceridine vs Sufentanil for Cough During Anesthesia Induction

Recruiting Phase 4
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Record status
This record was last updated July 21, 2026 (before its estimated July 25, 2026 completion). Its status may not reflect the trial's current state.
Summary
Sufentanil is the most widely used opioid analgesic for general anaesthesia induction; however, rapid intravenous bolus injection frequently triggers sufentanil-induced cough (SIC). In high-risk patients, SIC can cause abrupt elevation of intracranial and intraocular pressure and severe haemodynamic instability, posing a meaningful safety risk during the induction period. Oliceridine, the first G protein-biased μ-opioid receptor agonist approved by the Food and Drug Administration in 2020, provides analgesia through μ-receptor activation while substantially reducing β-arrestin-2 recruitment. This biased signalling profile is hypothesised to raise the excitation threshold of airway C-fibres and thereby reduce the incidence of cough. This prospective, single-centre, randomised, double-blind, parallel-group controlled trial directly compares oliceridine with sufentanil for general anaesthesia induction with respect to cough incidence, cough severity, haemodynamic responses, and perioperative safety, with the aim of providing evidence-based guidance for opioid selection during induction.
Protocol Amendment History 3 changes
critical Recruitment opened 2026-07-22
notable Primary completion moved earlier: 2026-08-25 -> 2026-07-01 2026-06-24
minor Completion moved earlier: 2026-08-30 -> 2026-07-01 2026-06-24
Trial Details
NCT Number NCT07660380
Lead Sponsor Shiyou Wei
Collaborators: Tianmen First People's Hospital
Conditions Cough, Anesthesia
Enrollment 62 participants
Start Date 2026-06-27
Primary Completion 2026-07-25 (estimated)
Study Completion 2026-07-28 (estimated)
Updated on ClinicalTrials.gov 2026-07-21