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A Study to compare different doses Dexmeditomidine in reducing haemodynamic in reducing haemodynamic response in laparoscopic surgeries.

A Randomised Prospective Comparative study of different doses of Dexmeditomidine in attenuating in haemodynamic response to pneumoperitoneum and post operative recovery in patients undergoing laparoscopic surgeries. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/090854
Enrollment
90
Registered
2025-07-14
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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: Different doses of intravenous Dexmeditomidine infusion in attenuating haemodynamic responses to pneumoperitoneum and post Operative recovery in patients undergoing laparoscopic surgeri

Sponsors

Chaithra V P
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All ASA grade 1 and 2 patients with BMI more than 18.5kg per meter square and less than 28kg per metre square, posted for elective laparoscopic surgery under general anaesthetia.

Exclusion criteria

Exclusion criteria: Patients with ischemic heart disease, uncontrolled diabetes mellitus, asthma, COPD, uncontrolled hypertension,chronic renal disease and liver diseases. Pregnant woman or lactating woman. Patients with anticipated difficulty airway. Patients with ASA grade 3 or more.

Design outcomes

Primary

MeasureTime frame
Changes in haemodynamic parameters- Heart rate, systolic blood pressure, diastolic blood pressure, mean arterial pressure at intubation, during pneumoperitoneum and at extubation. Cough reflex, shivering and sedation score post operatively.Timepoint: Changes in haemodynamic parameters- HR,SBP,DBPand MAP at baseline,at the end of Dexmeditomidine infusion,1 and 5 min after intubation,before creating pneumoperitoneum,5,15,30,45,60,90 min after creating pneumoperitoneum, at the end of pneumoperitoneum and before extubation, after extubation, 5 min and 20 min after extubation. Cough reflex, shivering and sedation score at extubation,20 min,2 hrs and 6hrs after extubation post operatively.

Secondary

MeasureTime frame
VAS score and first rescue analgesia post operatively. Adverse effects like Hypotension, bradycardia, PONV.Timepoint: First rescue analgesia after completion of surgery VAS more than 4 Hypotension, bradycardia, PONV at extubation, 20min, 2hr and 6hr.

Countries

India

Contacts

Public ContactKokila N

Mysore medical college and Research institute.

kokila222008@gmail.com9902357802

Outcome results

None listed

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