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Distal ischemic preconditioning for hypertensive vascular dysfunction: a double blind randomized clinical trial based on sham intervention control

Distal ischemic preconditioning for hypertensive vascular dysfunction: a double blind randomized clinical trial based on sham intervention control

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043024
Enrollment
Unknown
Registered
2021-02-04
Start date
2021-03-01
Completion date
Unknown
Last updated
2021-05-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Essential Hypertension

Interventions

Treatment group :Remote ischemic preconditioning
sham controlled group :sham controlled treatment

Sponsors

Department of Hypertension and Vascular Disease, the First Affiliated Hospital of Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients between 18 and 80 years old with essential hypertension; 2. Patients with grade 1 blood pressure rise or normal high value; 3. Subjects without smoking history or quitting smoking for more than one year; 4. Subjects without history of psychotropic drug use; 5. Subjects without caffeine intake during the study period; 6. Patients who signed informed consent and were willing to cooperate with the study.

Exclusion criteria

Exclusion criteria: 1. Patients with limb fracture, trauma, infection, arteriovenous fistula, etc; 2. Pregnant or lactating women; 3. Subjects with history of coronary heart disease, valvular heart disease, heart failure, diabetes, peripheral vascular disease, or patients with active inflammatory disease, malignant tumor and other serious diseases requiring treatment (such as acute liver disease, chronic renal failure, etc.); 4. Those patients with splenectomy; 5. Those patients who are not conducive to long-term follow-up or poor compliance; 6. Patients considered unsuitable for the trial by the researchers.

Design outcomes

Primary

MeasureTime frame
Office Blood Pressure;

Countries

China

Contacts

Public ContactJun Tao

Department of Hypertension and Vascular Disease, the First Affiliated Hospital of Sun Yat-Sen University

taojungz123@163.com+86 13922191609

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026