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Comparison Of Two Drugs For Avoidance Of Rise In Heart Rate And Blood Pressure While Securing The Airway At Start Of Anaesthesia

Comparative Study Of Clonidine & Esmolol In Attenuation Of Hemodynamic Stress Response To Endotracheal Intubation - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/061942
Enrollment
90
Registered
2024-01-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: K802- Calculus of gallbladder without cholecystitis

Interventions

Intervention1: Clonidine: 30 patients will be given intravenous infusion Clonidine, 2 mcg/kg, diluted in 20 ml of normal saline, slowly over 10 minutes before induction Intervention2: Esmolol: 30 pati

Sponsors

KPC Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Adult patients undergoing elective laparoscopic surgery 2. American Society Of Anesthesiologists Grade 1 3. Patients giving Informed Written, Valid consent

Exclusion criteria

Exclusion criteria: 1. Age less than 18 years and more than 45 years 2. Known allergy to anaesthetic agents 3. History of substance abuse and current opioid use 4. Anticipated difficult intubation 5. Duration of laryngoscopy more than 15 seconds 6. Baseline pulse less than 60 beats per minute 7. Baseline systolic blood pressure less than 100 mm Hg 8. Surgery time exceeding 2 hours 9. Pregnancy

Design outcomes

Primary

MeasureTime frame
The primary aim of the study is to compare the efficacy of Clonidine and Esmolol in attenuation of hemodynamic stress response due to laryngoscopy and endotracheal intubation.Timepoint: Rate Pressure Product (RPP) will be recorded just after intubation

Secondary

MeasureTime frame
The secondary aim of the study is to compare the efficacy of Clonidine & Esmolol in attenuation of hemodynamic stress response during pneumoperitoneum.Timepoint: Rate Pressure Product (RPP) will be recorded 5 minutes after pneumoperitoneum

Countries

India

Contacts

Public ContactDR Debjani Gupta

KPC Medical College & Hospital

debjani258@gmail.com9830071577

Outcome results

None listed

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