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A Comparative Study To attenuate stress response between intravenous dexmedetomidine and fentanyl.

Comparison Between Intravenous Dexmedetomidine Versus Intravenous Fentanyl In Attenuating the Hemodynamic Responses to Direct Laryngoscopy and Intubation in Adult Patients Undergoing Elective Surgeries under General Anaesthesia: An Observational Study in a Tertiary Care Centre in Mandya

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/075216
Enrollment
60
Registered
2024-10-14
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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: Dexmedetomidine: In my study I will be dividing patients into two groups Group D receives inj.dexmedetomidine and Group F receives Fentanyl As dexmedetomidine causes bradycardia , duri

Sponsors

Dr Somsundar R G
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients who are willing to give consent, patients requiring general anesthesia and intubation,

Exclusion criteria

Exclusion criteria: Patients ASA # and ASA 4,uncontrolled systemic disease, below 18 years,

Design outcomes

Primary

MeasureTime frame
To compare the efficacy of two different drugs dexmedetomidine (0.5mcg/kg) and Fentanyl 2mcg/kg for attenuation of hemodynamic response to laryngoscopy and endotracheal intubation.Timepoint: Baseline, before induction, before intubation, 1min after incubation, 3min after incubation, 5min after incubation and 10min after incubation.

Secondary

MeasureTime frame
To determine drug dependent side effects like hypotension, and bradycardia between two different drugs.Timepoint: 30mins

Countries

India

Contacts

Public ContactDr Somsundar R G

Mandya institute of medical sciences

somurg@gmail.com9686508877

Outcome results

None listed

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