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Long-term-opioid-free Anesthesia in Anterior Cervical Surgery

NCT05548465 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2024-05-07

No results posted yet for this study

Summary

We design this randomized controlled trial to explore the safety and efficacy of the long-term-opioid-free anesthesia in anterior cervical surgery, to reduce the dosage of perioperative long-acting opioids and promoting patients'rehabilitation.

Conditions

  • Long-term-opioid-free Anesthesia

Interventions

DRUG

Remifentanil Hydrochloride

Subjects will receive remifentanil anesthesia for operative analgesia.

DRUG

Sufentanil Citrate

Subjects will receive sufentanil and remifentanil anesthesia for operative analgesia.

Sponsors & Collaborators

  • West China Hospital

    lead OTHER

Principal Investigators

  • Ren Liao, M.D · West China Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-09-26
Primary Completion
2023-10-31
Completion
2023-12-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05548465 on ClinicalTrials.gov