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Comparing changes in Heart rate, Blood Pressure, Oxygen, Carbon dioxide levels and Narcotic Sparing Effect of Inhalation versus Intravenous Dexmeditomidine and Intravenous Fentanyl in laparoscopic surgeries under general anaesthesia

Comparison of haemodynamics and opioid sparing effect of dexmeditomidine nebulization and intravenous dexmeditomidine in laparoscopic surgeries under general anaesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/11/021920
Enrollment
90
Registered
2019-11-07
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: -

Interventions

Intervention1: Nebulization Dexmeditomidine Intravenous Dexmeditomidine Intravenous Fentanyl: In Laparoscopic Surgeries Under General Anaesthesia, Comparing Haemodynamics and Opioid Sparing Effect Of

Sponsors

Rajarajeswari Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Adult patients of either sex aged 18-65years 2 ASA 1 AND 2 3 Undergoing laparoscopic surgeries under general anaesthesia

Exclusion criteria

Exclusion criteria: 1 Patient refusing to participate in the study 2 Patient with uncontrolled diuabetes hypertension cardioresp[iratory neuropsychiatric disorders hepatic or renal dysfunction 3 BMI more than 30 and individual with difficult airway 4 Allergy to the study drug 5 Patient on medications like opiods sedatives beta blockers 6 Pregnant or lactating mother

Design outcomes

Primary

MeasureTime frame
Comparison of haemodynamic changes by dexmeditomidine nebulization with intravenous single dose dexmeditomidine and fentanyl in laparoscopic surgeries under general anaesthesiaTimepoint: Heart rate,Blood presure,Oxygen saturation, End tidal carbon dioxide will be observed 5 minutes after Premedication, 2 minutes post Induction, 5 minutes post Intubation Every 15 minutes post pneumoperitoneum, After extubation, Postop after 1hour—

Secondary

MeasureTime frame
Comparison Of Propofol Requirement Between The Study Groups To STUDY THE SAFETY PROFILE OF ABOVE AGENTSTimepoint: Requirement of Propofol At The Time Of Induction After Premedication—

Countries

India

Contacts

Public ContactDr Shankar K

Rajarajeswari Medical College and Hospital

shankarkraj111@gmail.com9740843854

Outcome results

None listed

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