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A Clinical Trial to Compare And Study The Effects Of Enhanced Recovery After Surgery (ERAS) Protocol Vs Conventional Care In Patients Undergoing surgery For Brain Aneurysm

Comparison Of Enhanced Recovery After Surgery(ERAS) Protocol Vs Conventional Care In Patients Undergoing Elective Craniotomy For Intracranial Aneurysms: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/10/037409
Enrollment
46
Registered
2021-10-20
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Health Condition 1: I671- Cerebral aneurysm, nonruptured Health Condition 2: I609- Nontraumatic subarachnoid hemorrhage, unspecified

Interventions

Intervention1: ERAS protocol in perioperative period: Patients will be counselled regarding the risk and benefit of the surgery and for abstinence from both alcohol and smoking when admitted. They wil

Sponsors

All india institute of medical sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient who gives Informed Consent 2.Patients with anterior circulation aneurysms with World Federation of Neurosurgical Societies(WFNS) grade 1 3.ASA grade 1 and 2 4.GCS 15/15

Exclusion criteria

Exclusion criteria: 1.Patients not giving consent 2.Patients with posterior circulation aneurysm 3.World Federation of Neurosurgical Societies (WFNS) grade 2,3,4 and 5 4.Age less than 18 years and more than 65 years 5.ASA grade 3,4,5 6. Pregnant patients 7. Patient requiring postoperative ventilation 8. History of previous brain surgery 9. Preoperative cognitive dysfunction 10. BMI > 40

Design outcomes

Primary

MeasureTime frame
length of stay in hospitalTimepoint: at discharge

Secondary

MeasureTime frame
Analgesic requirementTimepoint: In Postoperative period at 24 hours;Antiemetic requirement in 24 hoursTimepoint: In Postoperative period at 24 hours;Fentanyl consumption Timepoint: In intraoperative period;Functional recoveryTimepoint: discharge,1 month and 3 months;Length of ICU stayTimepoint: duration of stay in ICU after surgery;Pain assessment by Numerical Rating Score (NRS) pain scoreTimepoint: In Postoperative period at every 2 hour interval for 24 hours;Patient satisfaction scoreTimepoint: discharge;postoperative complications both surgical(surgical site infection, intracranial infection, epilepsy, haemorrhage, rebleeding , vasospasm etc) and non-surgical complications (respiratory complications, cardiovascular complications gastrointestinal complications, urinary tract complications, and venous thromboembolism etc )Timepoint: at discharge

Countries

India

Contacts

Public ContactDr Sneha Pandit

All India Institute Of Medical Sciences

dr.indu.me@gmail.com9013439134

Outcome results

None listed

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