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Study on Opioid-free Anesthesia Protocol With S-ketamine and Propofol

NCT05242081 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 980

Last updated 2022-07-20

No results posted yet for this study

Summary

The purpose of this study was to observe the effects of opioid-free anesthesia with S-ketamine on postoperative analgesia and perioperative hemodynamics in short surgical operations, and to explore the effects of S-ketamine on postoperative awakening time and extubation time, nausea and vomiting, hypoxemia, and delirium.

Conditions

  • Opioid Use, Unspecified
  • S-ketamine

Interventions

DRUG

S-ketamine

S-ketamine 0.5mg/kg for induction and 0.2mg/kg/h for maintenance

DRUG

Sufentanil

Sufentanil 0.2-0.3μg/kg for induction and remifentanil 0.05-0.15μg/kg/min for maintenance

Sponsors & Collaborators

  • The First Affiliated Hospital with Nanjing Medical University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2022-07-31
Primary Completion
2022-12-31
Completion
2023-06-30

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 NCT05242081 on ClinicalTrials.gov