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A comparison between Ivabradine (oral) and Labetalol(oral) for decreasing response to laryngoscope and intubation in laparoscopic abdominal surgery

Comparative evaluation of oral ivabradine and oral labetalol for attenuation of hemodynamic response to laryngoscopy and tracheal intubation in laparoscopic abdominal surgery - A prospective randomized comparative double blind studyâ??

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/054194
Enrollment
90
Registered
2023-06-20
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

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: O- Medical and Surgical

Interventions

Intervention1: Oral Labetalol: 200 mg of oral Labetalol 120 minutes before induction of anaesthesia. Control Intervention1: Oral Ivabradine: 5 mg of oral ivabradine 120 minutes before induction of ana

Sponsors

Muthu Vignesh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of ASA status 1 and 2 2. Patients with airway of Mallampati grade 1 and 2 3. Patients undergo elective laparoscopic abdominal surgery under general anaesthesia

Exclusion criteria

Exclusion criteria: 1. Patients refusal for study 2. Patients of ASA physical status 3 and 4 3. Allergy to drugs under study 4. Patients with significant bradycardia, hypotension and conduction blocks 5. Patients with cardiac, hepatic and renal disorders 6. Patients with anticipated difficult intubation (Mallampati grade 3 and 4) and requiring two attempts and more than 15 seconds at intubation 7. Patients receiving treatment with either of the drug under study

Design outcomes

Primary

MeasureTime frame
To assess & compare the changes in hemodynamic parameters of oral ivabradine & oral labetalol during laryngoscopy & endotracheal intubation.Timepoint: 2 hours before induction of anaesthesia to 4 hours after induction or desufflation whichever comes later.

Secondary

MeasureTime frame
To assess the side effects in the form of hypotension, bradycardia & any possible side effects if anyTimepoint: 2 hours before induction of anaesthesia to 4 hours after induction or desufflation whichever comes later.

Countries

India

Contacts

Public ContactArvind Kumar

Indira Gandhi Institute of Medical Sciences

arvind007kumar@yahoo.com9534870908

Outcome results

None listed

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