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NCT05910242Completed

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

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

Source: ClinicalTrials.gov · Last updated 3 Jun 2025

Brief summary (registry, in English)

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

Status (registry)
Completed
Study type
Interventional
Enrollment
102 (actual)
First submitted
7 Jun 2023
Start date
Jun 2023
Primary completion date
Mar 2024
Lead sponsor
Yi Yang
NCT number
NCT05910242

What you commit to

  • Study type: Interventional
  • Participants enrolled: 102
  • From Jun 2023 to the primary completion date, Mar 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Individuals who will or have received anticoagulant therapy with drugs such as dabigatran, rivaroxaban, warfarin, etc; ;
  • 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 illness

  • Secondary hypertension;
  • 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;
  • Other conditions that the researchers think are not suitable for the project.

Other

  • Clinical blood pressure ≥ 180/110 mmHg or 24-hour mean arterial pressure ≥ 170/100 mmHg;
  • Pregnant or lactating women;

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The First Hospital of Jilin University
Coordinator of this site? Confirm its status
ChangchunChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.