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Clinical trial

Safety and Efficacy of Remote Ischemic Conditioning in Patients With Essential Hypertension (SERIC-EH)

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Last updated:1st Nov 2022
Status: NOT YET RECRUITING
Identifier: https://clinicaltrials.gov/study/NCT03945305
Safety and Efficacy of Remote Ischemic Conditioning in Patients With Essential Hypertension (SERIC-EH)


ClinicalTrials.gov ID: NCT03945305
Sponsor: Yi Yang
Information provided by: Yi Yang, The First Hospital of Jilin University (Responsible Party)
Last Update Posted: 2022-11-02

Brief Summary:
The purpose of this study is to determine the efficacy and safety of remote ischemic conditioning for essential hypertension.

Detailed Description:
In this study, 1000 cases of essential hypertension in changping district, Beijing, who are currently taking oral antihypertensive drugs and still have poor blood pressure control (> 130/80mmHg) are included. The duration of the study is 3+ (30±2) days, during which time the changing of antihypertensive drugs are avoided and the types and doses of drugs taken daily are recorded. Baseline blood pressure and heart rate are measured 2 times a day for 3 days. And then the blood pressure and heart rate are measured before and after remote ischemic conditioning for 200mmHg, twice a day, 30±2 days in a row to evaluate the efficacy and safety of remote ischemic conditioning on essential hypertension.

Official Title:
Safety and Efficacy of Remote Ischemic Conditioning in Patients With Essential Hypertension

Intervention / Treatment:
Device: Remote Ischemic Conditioning

Category Value
Study Start (Actual) 2023-01-03
Primary Completion (Estimated) 2025-07-31
Study Completion (Estimated) 2025-07-31
Enrollment (Estimated) 1000
Study Type Interventional
Phase Not Applicable
Other Study ID Numbers

SERIC-EH

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