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To evaluate the haemodynamics, recovery profile and cost effecacy of Clonidine and Dexmedetomidine in patient undergoing laproscopic surgery.

A, PROSPECTIVE, RANDOMIZED, DOUBLE BLIND ,COMPARATIVE STUDY OF BIS GUIDED EVALUATION OF DEXMEDETOMIDINE AND CLONIDINE ON HAEMODYNAMICS, RECOVERY PROFILE AND COST EFFICACY IN PATIENTS UNDERGOING LAPAROSCOPIC SURGERY UNDER SEVOFLURANE ANAESTHESIA

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2011/05/001773
Enrollment
90
Registered
2011-05-31
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- laproscopic surgery

Interventions

Intervention1: Saline: This group will recieve 100 ml of normal saline over 10 minutes folowed by infusion of plain saline started 5 min after anaesthesia induction and continued till the application

Sponsors

Max Super Speciality Hospital a Unit of Balaji Medical Diagnostic Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Male or female Age between 18 to 55 years at the time of enrollment. 2.Scheduled for elective laparoscopic surgery under general anesthesia 3.ASA physical status I-II 4.Fit for anesthesia 5.Patients who have willingness to participate and provided written informed consent. 6.Ready to comply all schedule of approved protocol.

Exclusion criteria

Exclusion criteria: 1.Uncontrolled hypertension/ diabetes mellitus. 2.Severe hepatic/ respiratory/renal disease. 3.History of congestive cardiac failure, Type II/III heart block. 4.History of allergy to any of the test drugs. 5.Pregnancy or breast feeding female 6.History of opioid / alcohol intake in last 24 hrs. 7.Patients receiving á 2 agonists & Beta Blocker 8.Other medical, psychiatric, or behavioral limitations that in the judgments of the investigators may interfere with study participation or the ability to follow the intervention protocol.

Design outcomes

Primary

MeasureTime frame
1.To evaluate effect of clonidine and dexmedetomidine on haemodynamic response in patients undergoing laparoscopic surgeries under sevoflurane anaesthesia 2.To evaluate the recovery characteristics. 3.To find the cost efficacy of clonidine and dexmedetomidine in patients undergoing laparoscopic surgeries under sevoflurane anaesthesia Timepoint: Thease outcome will measures during pre anaesthesia after consent, during anaesthesia and Post anaesthesia till discharge from parameter mentioned in the protocol.—

Secondary

MeasureTime frame
Intra operative requirement of NM blocker Duration of Surgery Duration of anesthesia Timepoint: At interventional and post Interventional period—

Countries

India

Contacts

Public ContactArun Puri
arun.puri@maxhealthcare.com011-43033333

Outcome results

None listed

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