Efficacy and Safety of Non-sedation Trial in Patients After Neurosurgical Craniotomy

NANot yet recruitingINTERVENTIONAL
Enrollment

65

Participants

Timeline

Start Date

January 1, 2025

Primary Completion Date

June 30, 2026

Study Completion Date

December 31, 2026

Conditions
CraniotomyNeurosurgical Patients
Interventions
DRUG

non-sedation strategy

Patients eligible for this study will undergo non-sedation strategy, which continuous analgesia without sedation is performed with remifentanil. The remifentanil will be titrated (from 0.1µg/kg/min to 0.2ug/kg/min) every 10-15 minutes to achieve the goal for sedation (RASS score maintaining -2 to + 1). The patients in the non-sedation trial do not receive any sedatives but could receive bolus doses (2.5 or 5mg) of morphine for analgesia.

Trial Locations (1)

Unknown

Beijing Tiantan Hospital, South 4th Ring West Road 119, Fengtai District, Beijing 100070, China., Beijing

All Listed Sponsors
lead

Beijing Tiantan Hospital

OTHER

NCT06727435 - Efficacy and Safety of Non-sedation Trial in Patients After Neurosurgical Craniotomy | Biotech Hunter | Biotech Hunter