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Completed

NCT Number: NCT05910242

Efficacy and Safety of Remote Ischemic Conditioning in the Treatment of Essential Hypertension (RICBP-EH)

The purpose of this study is to determine the efficacy and safety of remote ischemic conditioning in the treatment of essential hypertension.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The First Hospital of Jilin University

Changchun, Jilin, 130000, China

About this study

Current studies have shown that remote ischemic conditioning can improve vascular endothelial function, inhibit sympathetic nervous system activity and regulate immune and inflammatory reactions. Thus it may exert anti-hypertensive effects through multiple mechanisms. The purpose of this study is to investigate the efficacy and safety of remote ischemic conditioning on blood pressure patients with essential hypertension.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age≥18 years, regardless of sex;
  • Patients with systolic blood pressure ≥140mmHg with or without taking oral antihypertensive drugs
  • Signed and dated informed consent is obtained

Exclusion criteria

  • Secondary hypertension;
  • Clinical blood pressure ≥ 180/110 mmHg or 24-hour mean arterial pressure ≥ 170/100 mmHg;
  • Severe organ dysfunction or failure;
  • Severe hematologic disorders or significant coagulation abnormalities;
  • History of atrial fibrillation or myocardial infarction within 6 months;
  • Individuals who had contraindication of remote ischemic conditioning, such as severe soft tissue injury, fracture or vascular injury in the upper limb, acute or subacute venous thrombosis, arterial occlusive disease, subclavian steal syndrome, etc;
  • Individuals who will or have received anticoagulant therapy with drugs such as dabigatran, rivaroxaban, warfarin, etc; ;
  • Pregnant or lactating women;
  • Those who are participating in other clinical research or has participated in other clinical research or has participated in this study within 3 months prior to enrollment;
  • Other conditions that the researchers think are not suitable for the project.

Treatment and study plan

Remote Ischemic conditioning

Procedure

Remote ischemic conditioning (RIC) is induced by 4 cycles of 5 min of upper limb ischemia followed by 5 min reperfusion. Limb ischemia was induced by inflation of a blood pressure cuff to 200 mm Hg.

Sham remote ischemic conditioning

Procedure

Sham-RIC is induced by 4 cycles of 5 min of upper limb ischemia followed by 5 min reperfusion. Limb ischemia was induced by inflation of a blood pressure cuff to 60 mm Hg.

Primary outcomes

  1. Mean systolic blood pressure

    Time frame: 1-7 days

    Difference in mean systolic blood pressure during RIC/sham-RIC between two groups.

Secondary outcomes

  1. Mean diastolic blood pressure

    Time frame: 1-7 days

    Difference in mean diastolic blood pressure during RIC/sham-RIC between two groups.

Sponsors and collaborators

Lead sponsor

Yi Yang

Other

Registry information

Official study title

Efficacy and Safety of Remote Ischemic Conditioning in the Treatment of Essential Hypertension

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Jun 18, 2023
Registry last updated
Jun 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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