Effect of clonidine in reducing blood pressure in hypertensive urgency situatio

Not Applicable

• Conditions: Hypertension.; Hypertensive diseases; I10-15

• Registration Number: IRCT2015122713828N7
• Lead Sponsor: Islamic Azad University, Najafabad branch,Isfahan

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 88

Inclusion Criteria

emergency hypertension; patients' agreement to participate.
Exclusion criteria: end organ damage; patients' non compliance; allergy to Clonidine or Captopril.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
High Blood Pressure. Timepoint: 15 minutes after treatment. Method of measurement: Sphygmomanometer.;Blood pressure. Timepoint: 15 min after treatment. Method of measurement: Sphygmomanometer.

Secondary Outcome Measures

Name	Time	Method
Dry mouth. Timepoint: 15 min after intervention. Method of measurement: Examination.;Headache. Timepoint: 15 min after intervention. Method of measurement: Examination.;Dizziness. Timepoint: 15 min after intervention. Method of measurement: Examination.;Palpitation. Timepoint: 15 min after intervention. Method of measurement: Examination.;Cough. Timepoint: 15 min after intervention. Method of measurement: Examination.;Angioedema. Timepoint: 15 min after intervention. Method of measurement: Examination.