Health Trials

Do Increasing Preoperative Timing of Single Dexmedetomidine Dose Have an Effect on Stress Response of Laryngoscopy and Intubation?

ConditionsTimeDexmedetomidineStress ResponseLaryngoscopyIntubation
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorTanta University

About this trial

This study aims to evaluate the effect of increasing preoperative timing of single dexmedetomidine on the stress response of laryngoscopy and intubation.

Eligibility criteria

Qualifiers

Age from 18 to 65 years.

Both sexes.

American Society of Anesthesiology (ASA) physical status I-II.

Disqualifiers

Severe cardiovascular problems.

Respiratory disorders.

Diabetes.

Hypertension.

Trial design

Treatments tested in this trial

  • Dexmedetomidine
  • Dexmedetomidine
  • Saline

Treatment groups

45 Participants
are divided into 3 treatment groups

Sponsors and collaborators

Tanta University

Lead sponsor

Source ClinicalTrials.gov