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Comparison of impact of use of inhalational and intravenous anaesthetic drugs on the outcome of aneurysmal clipping surgery.

Phase 3
Active, not recruiting
Conditions
Medical and Surgical,
Registration Number
CTRI/2023/07/054635
Lead Sponsor
Postgraduate Institute of Medical Education and Research
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
Inclusion Criteria

Ruptured aneurysm posted for Surgical Clipping WFNS grade 1,2,3 Anterior circulation aneurysm.

Exclusion Criteria

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
NameTimeMethod
To compare the incidence of delayed cerebral ischemia in patients undergoingstarting 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 comparedstarting after the surgery till the discharge from hospital
Secondary Outcome Measures
NameTimeMethod
Estimation of CSF eNOS levelsintraoperative ( 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, India
Dr Prudhvi Raj Veparala
Principal investigator
9500918238
Prudhviofficialmail@gmail.com

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