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To Study Haemodynamic Effects Of Preoperative Single Bolus Of Dexmedetomidine In Elective Laparoscopic Surgeries

Study Of Haemodynamic Effect Of Preoperative Single Bolus Of Dexmedetomidine In Elective Laparoscopic Surgeries - Lap Dex

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/07/034890
Enrollment
60
Registered
2021-07-15
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: K352- Acute appendicitis with generalized peritonitis Health Condition 2: K800- Calculus of gallbladder with acutecholecystitis

Interventions

Intervention1: General Anaesthesia in Laparoscopic surgeries: GENERAL ANAESTHESIA TECHNIQUE All the patients will be kept nil per oral (NPO) for a period of atleast 6hrs prior to surgery to avoid the

Sponsors

Department of Anaesthesia
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade I and II patients undergoing elective laparoscopic surgeries under general anaesthesia Haemodynamically stable patietns availability of informed consents

Exclusion criteria

Exclusion criteria: Patient refusal ASA III and more age below 18 and above 60 patients posted for emergency surgeries patients who are on drugs that can influence haemodynamic and autonomic functions predictable difficult airway or difficult intubation pre existing heart condition pregnancy and breast feeing women co-existing illness like respiratory, renal or cerebral diseases surgeries converted to open surgeries known allregy to any of the drugs used in the study

Design outcomes

Primary

MeasureTime frame
to study the effects of dexmedetomidine on hemodynamic parameters during perioperative periods in patients undergoing elective laparoscopic surgeriesTimepoint: Every 5 minutes post induction

Secondary

MeasureTime frame
to study post operative sedation score using ramsay sedation scaleTimepoint: 6 hours;To study the side effects of Dexmedetomidine and their managementTimepoint: Every 5 minutes post induction ;To study the time taken for the first analgesic requirement.Timepoint: 12 hours

Countries

India

Contacts

Public ContactDr Mary Samuel

Dr D Y Patil Medical College Hospital and Research Centre

Fthm_93@yahoo.com9096410540

Outcome results

None listed

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