Skip to content

Optimizing Respiratory Health in COPD Patients: The Role of Pre-Operative Ketamine (Nebulized vs. IV) in Laparoscopic Surgery

Comparison of pre-operative nebulization with ketamine versus intravenous ketamine on respiratory parameters in COPD patients undergoing laparoscopic abdominal surgery: a randomized control trial - nil

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079005
Enrollment
62
Registered
2025-01-20
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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: IV KETAMINE: This will be the Primary group, to whom 0.4mg/kg iv ketamine (total volume 5ml) bolus + 0.4mg/kg infusion (total volume 100ml) &amp
nebulized saline will be administered Control Intervention1: NEBULIZED KETAMINE: This will be the Test Group, to whom nebulised ketamine (0.8mg/kg) & iv saline (5ml) bolus + infusion (100ml) will be a

Sponsors

All India Institute of Medical Sciences Jodhpur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with COPD undergoing laproscopic abdominal surgery under GA ( with et/i-gel) Age: 18-70 yrs Physical status : asa ii,iii Laproscopic abdominal surgery under GA lasting upto 2 hrs Patient willing to provide informed consent

Exclusion criteria

Exclusion criteria: Administration of preoperative iv steroid therapy Patients who have previously undergone any airway surgery Patients with allergy to study drug Patients with known cardiac disease

Design outcomes

Primary

MeasureTime frame
to compare the effectiveness of pre-operative ketamine nebulisation versus iv ketamine on changes in peak expiratory flow rate (PEFR) in COPD patients undergoing laparoscopic abdominal surgery.Timepoint: 30minuites of intervention

Secondary

MeasureTime frame
1)To compare the forced expiratory volume in 1(FEV1) second measured pre and post intervention 2)Assessment of post intubation bronchospasm . 3)Assessment of side effects of ketamine : salivation, lacrimation, hallucination etc.Timepoint: 30 minuites post intervention

Countries

India

Contacts

Public ContactLALHLIMPUII FANAI

AIIMS,JODHPUR

docbpali@gmail.com9588089378

Outcome results

None listed

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