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Dexmedetomidine vs Labetalol for attenuating hemodynamic responses during Laparoscopic Cholecystectomy in borderline hypertensives

Comparative evaluation of efficacy of Dexmedetomidine and Labetalol for attenuating hemodynamic responses during Laparoscopic Cholecystectomy in borderline hypertensive patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/09/009745
Enrollment
160
Registered
2017-09-13
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Borderline Hypertensives

Interventions

Intervention1: Dexmeditomidine: 0.5microgm/Kg i.v. Dexmeditomidine10 mins before induction of general anesthesia Control Intervention1: Labetalol: 0.5 mg/Kg i.v. Labetalol 10 mins before induction o

Sponsors

AIIMS Rishikesh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age between 20-60 years 2. Borderline controlled hypertensive (controlled NIBP 3. ASA physical status 4. Planned for laparoscopic cholecystectomy as elective surgery under general anaesthesia

Exclusion criteria

Exclusion criteria: 1. Patientsâ??s refusal 2. ASA grade IV 3. Patient taking any antihypertensive medication 4. Patients with ASA physical status of 3 or more 5. Age > 60 years & 6. Cardio-pulmonary compromised patients 7. Major hepatic, Renal or endocrine dysfunction 8. Allergy to anaesthetic drugs used.

Design outcomes

Primary

MeasureTime frame
To compare the efficacy of dexmedetomidine and labetalol on attenuation of pressure response during laryngoscopy and intubationTimepoint: Pre operative, 5,10 min. post drug administration, after Intubation, before pneumoperitoneum, post pneumoperitoneum at 10,20,30 minutes, release of CO2 and Extubation

Secondary

MeasureTime frame
To compare the safety profile in terms of incidence of various side effects such as bradycardia, hypotension, nausea, vomiting.Timepoint: Pre operative, 5,10 min. post drug administration, after Intubation, before pneumoperitoneum, post pneumoperitoneum at 10,20,30 minutes, release of CO2 and Extubation

Countries

India

Contacts

Public ContactDeepak Singla

AIIMS Rishikesh

deepak10.4u@gmail.com

Outcome results

None listed

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