Comparison of impact of use of inhalational and intravenous anaesthetic drugs on the outcome of aneurysmal clipping surgery.
- Conditions
- Medical and Surgical,
- Registration Number
- CTRI/2023/07/054635
- Brief Summary
This trial is designed to see the effect of anaesthesia drugs on the incidence of delayed cerebral ischemia in patients of aneurysmal subarachnoid haemorrhage undergoing surgical clipping of the neck of aneurysm. after randomly dividing into two groups, patients of one group will receive propofol( intravenous) as an anaesthetic agent, while the other will receive sevoflurane ( inhalational) as the anaesthetic agent. Postoperatively these patients are followed up to compare the incidence of Delayed cerebral ischemia between the two groups. Secondarily we reach CSF levels of the eNOS enzyme, collected at the time of surgery. we also check neurological outcomes using MRS scoring at discharge and both MRS and GOSE scale at 1 month and w3 months.w
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- All
- Target Recruitment
- 200
Ruptured aneurysm posted for Surgical Clipping WFNS grade 1,2,3 Anterior circulation aneurysm.
Postictal day 4 or more Postoperative neurological deterioration due to surgical or systemic causes Hydrocephalus.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the incidence of delayed cerebral ischemia in patients undergoing starting after the surgery till the discharge from hospital to propofol. starting after the surgery till the discharge from hospital clipping of aneurysm surgery under general anesthesia with sevoflurane when compared starting after the surgery till the discharge from hospital
- Secondary Outcome Measures
Name Time Method Estimation of CSF eNOS levels intraoperative ( during aneurysm Clipping surgery) Neurological outcome at discharge ( MRS score) at discharge Neurological outcome at 3 months post surgery(GOSE, MRS score) 1 months after surgery, 3 months after surgery
Trial Locations
- Locations (1)
Postgraduate Institute of Medical Education and Research
🇮🇳Chandigarh, CHANDIGARH, India
Postgraduate Institute of Medical Education and Research🇮🇳Chandigarh, CHANDIGARH, IndiaDr Prudhvi Raj VeparalaPrincipal investigator9500918238Prudhviofficialmail@gmail.com