Skip to content

Effect of Anaesthetic gas Sevoflurane on blood vessel following aneurysmal subarachnoid hemorrhage, in patients receiving nimodipine, assessed by radiology imaging :a prospective randomized controlled trial

Effect of Sevoflurane on vasospastic cerebral vasculature following aneurysmal sah, in patients receiving intra- arterial nimodipine, assessed by digital subtraction angiography :a prospective randomized controlled trial(SIAN-VCV trial) - SIAN-VCV

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/077510
Enrollment
62
Registered
2024-11-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: G00-G99- Diseases of the nervous system Health Condition 2: D80-D89- Certain disorders involving the immune mechanism Health Condition 3: G973- Intraoperative hemorrhage and hematoma of a nervous system organ or structure complicating a procedure Health Condition 4: G973- Intraoperative hemorrhage and hematoma of a nervous system organ or structure complicating a procedure Health Condition 5: G978- Other intraoperative and postprocedural complications and disorders of nervous

Interventions

Intervention1: Sevoflurane: Sevoflurane will be used in dose of 1- 1.3 MAC for induction and upto procedure completed. Effect on diameter of measure cerebral vessel will be noted by digital subtractio

Sponsors

Director PGIMER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults patients (age 18 yrs) with cerebral vasospasm following aneurysmal subarachnoid hemorrhage posted for intra-arterial nimodipine who are either unconscious,semiconscious,irritable or intubated and need for general anaesthesia for the procedure

Exclusion criteria

Exclusion criteria: 1. Patient or legal heir’s refusal for consent 2. Patient with H/O allergy to test drugs 3. Patient who received intraarterial Nimodipine previously. 4. Patients having deranged renal parameters 5. Patients with vasculitis. 6. Patient having hydrocephalus. 7. Patients having abnormal coagulation parameters

Design outcomes

Primary

MeasureTime frame
Effect on diameter of major cerebral vessels ICA,MCA,ACATimepoint: Baseline before giving general anesthesia and after nimodipine administration

Secondary

MeasureTime frame
1. To assess changes in Cerebral Arterio-Venous Transit Time which is a surrogate marker of the cerebral blood flow by DSA. 2. Cerebral blood flow velocity (SFV/DFV/MFV), Pulsatility Index (PI) and Lindegaard ratio measured by TCD, before the procedure, 1 hour and 24 hours after procedure. These parameters will be measured once daily again for 1-5 days after IA Nimodipine. 3. Total dose of intra-procedure nimodipine. 4. Requirement of additional doses of Intra-arterial nimodipine during ICU stay. 5. Development of cerebral infarction during ICU stay. 6. Neurological status of the patients at discharge by Modified Rankin score (mRS). Timepoint: 0 Days till discharge

Countries

India

Contacts

Public ContactSk Ahadul Islam

Post Graduate Institute of medical education and research

nidhibp@gmail.com7087009525

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026