Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05195034

Effect of Dexmedetomidine on Postoperative Delirium After Awake Craniotomies

Effect of Dexmedetomidine on Postoperative Delirium in Patients Undergoing Awake Craniotomies: a Randomized Controlled Trial

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
210 (estimated)
Sponsor
Beijing Tiantan Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Postoperative delirium (POD) is a common complication, and the incidence of POD ranges from 10% to 60%. Previous studies suggested that frontal approach and tumor located at the temporal lobe were independent risk factors for POD after supratentorial tumor resections. Therefore, patients undergoing awake craniotomies are high-risk populations for POD. A lot of trials show that dexmedetomidine might help to reduce the incidence of delirium in patients undergoing non-cardiac surgery. However, the impact of dexmedetomidine (DEX) on POD for patients undergoing awake craniotomies remains unclear. The purpose of this study was to investigate the effect of DEX on POD in patients undergoing awake craniotomies.

Conditions

Interventions

TypeNameDescription
DRUGDexmedetomidineThe 200ug dexmedetomidine will be diluted into a 50ml syringe and administered with continuous infusion at a rate of 0.2 µg/kg/hour until the end of dural closure.
DRUG0.9% salineThe 0.9% saline is administered with the same volume at the same speed as the other group.

Timeline

Start date
2022-03-31
Primary completion
2025-11-30
Completion
2025-12-31
First posted
2022-01-18
Last updated
2025-02-13

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05195034. Inclusion in this directory is not an endorsement.