CTRI/2025/04/084227Not yet recruitingNot Applicable
An analysis of clinical effects on supratentorial craniotomy surgery without neuromuscular blocking agents during maintenance phase of anaesthesia.
Dr Mohamed Anus Thoufeeque S1 site in 1 country50 target enrollmentStarted: April 16, 2025Last updated:
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 50
- Locations
- 1
- Primary Endpoint
- To elicit the clinical effects and physiological parameters during the maintenance phase of anaesthesia in patients undergoing supratentorial craniotomy surgery
Study Overview
Brief Summary
Neuromuscular blocking agents have been one of the cornerstones of anaesthesia.
When balanced anaesthesia with desflurane,dexedetomidine,propofol infusion and scalp block will prelude the use of neuromuscular blocking agents in patients undergoing supratentorial craniotomy surgery under intense hemodynamic monitoring.
Study Design
- Study Type
- Interventional
- Allocation
- Not Applicable
- Masking
- Not Applicable
Eligibility Criteria
- Ages
- 18.00 Year(s) to 60.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •American Society of Anaesthesiologists(ASA) physical status I & II, Glasgow Coma Score of 15, Undergoing elective craniotomy surgery for supratentorial lesions.
Exclusion Criteria
- •Refusal to consent, Known hypersensitivity to drugs being used, Pregnant and lactating patients, Sick sinus syndrome, Patients on beta blockers.
Outcomes
Primary Outcomes
To elicit the clinical effects and physiological parameters during the maintenance phase of anaesthesia in patients undergoing supratentorial craniotomy surgery
Time Frame: Outcomes will assessed during intraoperatively till the end of surgery and postoperatively for 1 hour.
Secondary Outcomes
- TO ASSESS THE TIME TAKEN FOR DISCHARGE FROM POST ANAESTHETIC CARE UNIT(POSTOPERATIVE PERIOD)
- To assess the time taken for discharge from the post anaesthetic care unit(Postoperatively for 1 hour)
Investigators
Study Sites (1)
Loading locations...
Similar Trials
Completed
Not Applicable
Safety and Feasibility of a New Neuromuscular Monitoring DeviceGeneral AnesthesiaNCT03847740Poitiers University Hospital15
Completed
Not Applicable
The Effect of Deep Neuromuscular Blockade on Requirement of Intravenous Anesthetic AgentGeneral AnesthesiaNeuromuscular BlockadeLaparoscopyNCT03890406Seoul National University Bundang Hospital88
Completed
Phase 4
0.6 vs. 1.2 mg Atropine Together With Neostigmine 2.5 mg on Heart Rate in Patient Receiving Muscle RelaxantBradycardiaNeostigmine Adverse ReactionAdverse Reaction to Belladonna or AtropineNCT02186132Mahidol University40
Completed
Phase 4
Deep Neuromuscular Block During General Anaesthesia in Robotic SurgeryObservation of Neuromuscular BlockComplication of Ventilation TherapyPostoperative RecoveryNCT03420937University Hospital Olomouc138
Completed
Not Applicable
Influence of anesthetics on neuromuscular blocking effect of adductor pollicis and corrugator supercilii musclespatients undergoing elective surgeryJPRN-UMIN000025413Kawasaki medical school30
