FindTrial
Sign In

Study of effect of intranasal ketamine on postoperative pain in children

Study of effect of intranasal ketamine on postoperative analgesia in children - A one year single blinded hospital based randomized placebo controlled clinical trial - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/055681
Enrollment
104
Registered
2023-07-25
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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: Ketamine: 1mg/kg of Intranasal Ketamine will be instilled with atomizer after the completion of the surgical procedure and once the closure starts. Control Intervention1: Normal saline:

Sponsors

DR APOORVA S
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.CHILDREN IN THE AGE GROUP 5 TO 18 YEARS UNDERGOING SURGERY UNDER GENERAL ANAESTHESIA 2. CHILDREN IN ASA GRADE I TO II

Exclusion criteria

Exclusion criteria: CHILDREN WITH 1. ALLERGIC TO STUDY DRUG 2. ASA GRADE III OR > III 3. ABERRANT NASAL ANATOMY THAT PRECLUDES INTRANASAL MEDICATIONS. 4. PATIENTS UNDERGOING ANY NASAL SURGERY

Design outcomes

Primary

MeasureTime frame
Assessement for postoperative pain after intranasal administration of ketamineTimepoint: At 15, 30,45,60 min, 2,6, 12, 24 hours post operatively using modified Childrenâ??s Hospital of Eastern Ontario Pain Scale (CHEOPS) and Visual Analog Scale—

Secondary

MeasureTime frame
To determine the total amount of analgesicTimepoint: Anagesia required in first 24 hours post operatively—

Countries

India

Contacts

Public ContactDR VANDANA GOGATE

KLE UNIVERSITY JAWAHARLAL NEHRU MEDICAL COLLEGE

vandanagogate@gmail.com98440830830

Outcome results

None listed

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