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Clinical Trials/CTRI/2016/01/006519
CTRI/2016/01/006519
Recruiting
Phase 4

â??CLINICAL EVALUATION OF EFFICACY AND SAFETY OF THREE DIFFERENT DOSES OF FENTANYL TO PREVENT HAEMODYNAMIC STRESS RESPONSE DURING LARYNGOSCOPY AND INTUBATION: A RANDOMIZED DOUBLE BLIND CLINICAL STUDYâ??

GOVERNMENT MEDICAL COLLEGE0 sites90 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
GOVERNMENT MEDICAL COLLEGE
Enrollment
90
Status
Recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • Age: 18 to 40 years.
  • Gender: Either gender.
  • Patients posted for elective surgery under general anaesthesia requiring endotracheal intubation.
  • Duration of surgery up to 2 hrs.
  • ASA physical status I and II.
  • BMI \<\= 25kg/m2\.
  • Informed written consent for participation in study.

Exclusion Criteria

  • Patients with diabetes, COPD, renal disease, cardiac diseases like IHD, hypertension, valvular heart disease, AV conduction block, aortic stenosis, left ventricular failure, etc.
  • Patients on drugs having effects on heart rate and blood pressure (sedatives, opioids, β\-blockers, calcium channel blockers, diuretics) and anti\-psychiatric drugs.
  • Pregnant women and lactating mothers.
  • Anticipated difficult intubation.
  • Intubation attempt lasting longer than 15 seconds.

Outcomes

Primary Outcomes

Not specified

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