Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06607029

Opioid-free Anesthesia Protocol for Neurosurgical Supratentorial Tumor Resection

Led by Beijing Tiantan Hospital · Updated on 2025-03-11

170

Participants Needed

1

Research Sites

75 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Opioids have many side effects, such as constipation, urinary retention, itchy skin, respiratory depression, and postoperative nausea and vomiting. These side effects can lead to delayed recovery, longer hospital stays, and increased health care costs. Opioid-free anesthesia is the combination of anti-nociceptive drugs to block the different pathways involved in the transmission of nociceptive information, control pain, avoid opioid-related adverse reactions, and promote patient recovery. At present, opioid-free anesthesia is not widely used in craniocerebral surgery in neurosurgery, and the relevant clinical data are extensive. Therefore, the investigators urgently need to conduct a randomized controlled study to provide clinical evidence for the efficacy and safety of opioid-free anesthesia in neurosurgical patients.

CONDITIONS

Official Title

Opioid-free Anesthesia Protocol for Neurosurgical Supratentorial Tumor Resection

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Scheduled for craniotomy for supratentorial tumors with general anesthesia
  • Aged 18 to 65 years
  • American Society of Anesthesiologists (ASA) physical status I to III
  • Signed informed consent
Not Eligible

You will not qualify if you...

  • Body mass index (BMI) 35 kg/m2 or higher
  • Severe liver or kidney failure
  • Cognitive dysfunction, aphasia, or inability to cooperate with assessments
  • Head MRI showing midline brain shift greater than 5 mm
  • Undergoing electrophysiological monitoring during surgery
  • Pregnant or breastfeeding

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Beijing Tiantan Hospital

Beijing, China

Actively Recruiting

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Research Team

H

Han

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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