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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03204006
Other study ID # 01003060483
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 8, 2018
Est. completion date March 12, 2020

Study information

Verified date March 2020
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Attenuation of Hemodynamic Response to Laryngoscopy and Endotracheal Intubation With Single Dose of Dexmedetomidine in Hypertensive Patients.


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date March 12, 2020
Est. primary completion date March 8, 2020
Accepts healthy volunteers No
Gender All
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria:

- - Age group 20-60 years

- ASA grade 1 and 2

- control hypertensive patients.

Exclusion Criteria:

- - Consent not given

- ASA Grade 3 and 4

- history of myocardial ischemia or infarction, or had an abnormal ECG on admission to the hospital

- Patients with cardiovascular, pulmonary, hepatic, and renal disease.

- Patients on B blockers.

- patients with difficult airway; laryngoscopy and intubation time more than 20 s, or requiring more than two attempts will be exclude from the study.

Study Design


Related Conditions & MeSH terms

  • Stress Response During Laryngoscopy Intubation

Intervention

Drug:
Dexmedetomidine
Dexmedetomidine preinduction
sterile saline
normal saline preinduction

Locations

Country Name City State
Egypt Assiut University Hospital Assiut

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary heart rate through first 15 min post-induction of anesthesia
Secondary systolic blood pressure through first 15 min post-induction of anesthesia
Secondary diastolic blood pressure through first 15 min post-induction of anesthesia