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Comparison Of Gastric Content In patients Fasting Vs patients given with Oral Rehydration Solution 2hours prior to surgery using Ultrasound machine placed on Stomach.

A Randomized Prospective Comparative Study Of Assessment Of Residual Gastric Volume By USG In Patients With Overnight Fasting Vs Administration Of Oral Re Hydration Solution 2 Hours Prior To The Surgery In A Tertiary Cancer Care Center

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/082518
Enrollment
60
Registered
2025-03-18
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Health Condition 1: C40-C41- Malignant neoplasms of bone and articular cartilage Health Condition 2: C00-C14- Malignant neoplasms of lip, oral cavity and pharynx Health Condition 3: C30-C39- Malignant neoplasms of respiratory and intrathoracic organs Health Condition 4: C43-C44- Melanoma and other malignant neoplasms of skin Health Condition 5: C45-C49- Malignant neoplasms of mesothelial and soft tissue Health Condition 6: C50-C50- Malignant neoplasms of breast Health Condition 7: C51-C58- Malig

Interventions

Intervention1: Administration of Oral rehydration solution 200ml 2 hours prior to the Surgery: Administration of Oral rehydration solution 2 hours prior to the surgery and assessment of residual gastr

Sponsors

Dr Bharath B
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients undergoing elective Surgery 2.age between 18 to 60 years 3.Patient who can provide consent 4.Accepted under ASA grade 1 and ASA grade 2

Exclusion criteria

Exclusion criteria: Patient refusal to the consent, patients with gastroesophageal reflux disease, patients accepted under ASA grade 3 and ASA grade 4, patients with uncontrolled diabetes mellitus, patients with GI obstruction.

Design outcomes

Primary

MeasureTime frame
To assess residual gastric volume by USG after administration of oral rehydration solution 2 hours prior to the surgeryTimepoint: 2 hours prior to the surgery

Secondary

MeasureTime frame
nilTimepoint: nil

Countries

India

Contacts

Public ContactDr Henjarappa K S

Kidwai Institute of Oncology, Bengaluru

drhenjarappa@gmail.com7019933746

Outcome results

None listed

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