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Recovery in planned neurosurgery in a group of patients

Enhanced recovery in elective supratentorial craniotomies- a randomised controlled study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/066005
Enrollment
150
Registered
2024-04-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: ERAS protocol: Abstinence from smoking and alcohol for 4 weeks before surgery, proton pump inhibitors preop, fasting 6h for light non fatty meal and 2h for clear liquids, scalp block, l

Sponsors

SIMS Hospitals
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1 and 2, patients admitted for elective craniotomy for a single intracranial supratentorial lesion

Exclusion criteria

Exclusion criteria: ASA 3 and 4, patients with major comorbid conditions, obese individuals with BMI more than or equal to 30, patients with drug allergies or egg allergy, patients participating in any other clinical studies, patient with major neurological deficits

Design outcomes

Primary

MeasureTime frame
Duration of hospital stay and total hospitalisation costTimepoint: From admission to discharge

Secondary

MeasureTime frame
Readmission rates, postoperative complications, postoperative pain scores, perioperative opioid consumption, length of ICU , duration of drainage tube, time to first oral intake, postoperative functional recovery statusTimepoint: 30 days from day of discharge

Countries

India

Contacts

Public ContactDr Magimairaj

SIMS Hospitals

mdavidjayapal@gmail.com9840757749

Outcome results

None listed

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