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Using Ultrasonography to Compare Stomach Fullness Before Brain Surgery in Two Groups: One Following a Fast-Track Recovery Plan and One Following the Usual Plan

Comparison of Preoperative Ultrasonographic Gastric Volume Assessment in Patients on ERAS protocol versus Conventional protocol undergoing Elective Intracranial Neurosurgery - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/091810
Enrollment
212
Registered
2025-07-28
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: D496- Neoplasm of unspecified behavior of brain

Interventions

Intervention1: Nil: Nil

Sponsors

Dr Ashish Patyal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Body mass index BMI greater than 35 kg per metre squared American Society of Anesthesiologists ASA classification 1 and 2 Patient with brain tumor with symptoms and signs of raised ICP Patient with GCS greater than 13 Schedule for elective intracranial neurosurgery

Exclusion criteria

Exclusion criteria: Any abnormal anatomy of the upper gastrointestinal system like previous esophagus or gastric surgery including hiatus hernia Patient with active gastric or duodenal ulcer and upper gastrointestinal system bleeding Patient with Vagal nerve denervation Patient on opioids less than 8 hrs duration Patient with infiltrative diseases such as scleroderma or amyloidosis Pregnant patients Patients with uncontrolled Diabetes Mellitus

Design outcomes

Primary

MeasureTime frame
To find the correlation between duration of fasting and gastric volume in patients with brain tumors, on ERAS protocol versus Conventional protocol.Timepoint: At Baseline

Secondary

MeasureTime frame
To assess & compare the effect on gastric emptying time on tumor location between the two groups.Timepoint: At baseline;To assess & compare the gastric emptying time in patients with comorbidities between the two groups ( DM , Hypertension etc).Timepoint: At baseline;To compare intra-operative blood glucose level between two groups .Timepoint: Intra-operatively at 1 hour from start of operation

Countries

India

Contacts

Public ContactDr Ashish Patyal

Geetanjali Medical College and Hospital

aspatyal501@gmail.com9004600184

Outcome results

None listed

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