Ketamine v/s Ketofol for short Sedation in Pediatric Patients

Comparative Study Between Ketamine and Ketofol for Procedural Sedation in Pediatric Patients - nil

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

CTRI

Registry ID

CTRI/2026/02/104513

Enrollment

108

Registered

2026-02-23

Start date

Unknown

Completion date

Unknown

Last updated

2026-03-02

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

Conditions

Health Condition 1: N00-N99- Diseases of the genitourinary system

Interventions

Intervention1: ketamine vs ketofol(ketamine and propofol combination): to compare total sedation time,time to recovery,hemodynamic parameters and side effects between 2 agents Intervention2: ketofol(k

Eligibility

Inclusion criteria

Inclusion criteria: ASA I And II Patients posted for U-Calibration, dressing under sedation for operated cases of genitourinary system defects.

Exclusion criteria

Exclusion criteria: ASA III, IV and V Age less than 1 year and more than 12 year Hypersensitivity to Propofol And Kitamine. Active rspiratory tract infection.

Design outcomes

Primary

Measure	Time frame
Compare the total sedation time in both group.Timepoint: 2,4,6,8,10,15,20 minutes till recovery.	—

Secondary

Measure	Time frame
Assess the Time to Recovery in both groups. Compare the adverse events in both groups. Additional Dose requirement in both groups. Hemodynamic parameters in both groups.Timepoint: 2,4,6,8,10,15,20 minutes till recovery.	—

Countries

India

Contacts

Public ContactDr. Nilesh solanki

b.j.medical college,civil hospital ,ahmedabad.

nmscbaps@gmail.com9998991716

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026