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Comparison of Ketamine-Dexmedetomidine (KETODEX) and Ketamine-Propofol (KETOFOL) for sedation during flexible bronchoscopy

The Effectiveness of comparision of Ketamine and Dexmedetomidine (KETODEX) infusion versus Ketamine and Propofol(KETOFOL) infusion for sedation during flexible bronchoscopy. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/091216
Enrollment
42
Registered
2025-07-21
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: J989- Respiratory disorder, unspecified

Interventions

Intervention1: KETODEX (IV infusion of Ketamine 4 mg/ml + Dexmedetomidine 4 mcg/ml): KETODEX (Intervention Group) Type of Product: Investigational combination of approved drugs Name of Product: KETOD

Sponsors

Shree Krishna Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1 ,2,3 Spontaneously breathing patients scheduled for flexible bronchoscopy under sedation

Exclusion criteria

Exclusion criteria: Allergy to ketamine, propofol, or dexmedetomidine Tracheostomized or intubated patients Patients with heart block or recent myocardial infarction Patients who convert to mechanical ventilation

Design outcomes

Primary

MeasureTime frame
To compare the effectiveness of Ketamine and Dexmedetomidine (Ketodex) vs. Ketamine and Propofol (Ketofol) for sedation during flexible bronchoscopy.Timepoint: post procedure for 1 hour—

Secondary

MeasureTime frame
To assess patient satisfaction, bronchoscopy satisfaction, coughing response of patient, assess the need for other drugs, assess the intraprocedure and post procedure complicationsTimepoint: Post procedure 1 hour—

Countries

India

Contacts

Public ContactDr Pruthil Patel

Pramukhswami Medical college, Bhaikaka University

Birvank@charutarhealth.org9537122077

Outcome results

None listed

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