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Investigating Optimal Approaches to Postoperative Nil by Mouth

Investigating Optimal Approaches to Postoperative Nil by Mouth: A Preliminary Exploratory Study in Paediatric Patients Protocol - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/03/081819
Enrollment
500
Registered
2025-03-06
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: - Health Condition 2: 8- Other Procedures

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

Institute of medical sciences, BHU
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Children aged 1 to 5 years undergoing daycare such as hernia, Opexy, circumcision Cystoscopy and Urethral Dilatation and Removal of moles, cysts, or other benign skin lesions

Exclusion criteria

Exclusion criteria: Exclusion Criteria: Surgeries with hospital stay,cavity invading surgeries, children prone to nausea and vomiting, and cases where parental consent is refused.

Design outcomes

Primary

MeasureTime frame
Incidence of POV in the immediate post operative periodTimepoint: Incidence of POV in the immediate post operative period—

Secondary

MeasureTime frame
1.time to first oral sip as per stewards score and time to first oral semisolid intake on demand 2. Pain score at 2, 4, 8, 12 and 24 hours using FLACC scale 3. Time to discharge 4. Parent satisfaction scale 5. Complications, if any Timepoint: Pain score at 2, 4, 8, 12 and 24 hours using FLACC scale—

Countries

India

Contacts

Public ContactAmrita Rath

Institute of medical sciences, Banaras Hindu University

amritar@bhu.ac.in07379140545

Outcome results

None listed

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