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Remote Ischemic Conditioning for the Treatment of Resistant Hypertension

Efficacy and Safety of Remote Ischemic Conditioning for the Treatment of Resistant Hypertension: a Pilot Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05426707
Enrollment
40
Registered
2022-06-22
Start date
2022-10-01
Completion date
2023-03-30
Last updated
2022-09-08

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

Conditions

Resistant Hypertension

Keywords

Resistant Hypertension, Remote ischemic conditioning

Brief summary

This study aims to explore the efficacy and safety of remote ischemia adaptation for the treatment of resistant hypertension.

Detailed description

Resistant hypertension is defined as a blood pressure of 140/90 mmHg or higher despite adherence to at least three antihypertensive drugs (including one diuretic), accounting for 20% to 30% of patients with hypertension. Compared with patients with well-controlled blood pressure, the cardiovascular risk of resistant hypertension is increased by about 50%. Limb remote ischemic conditioning (LRIC) triggers endogenous protective effects through transient and repeated ischemia in the limb to protect remote tissues and organs. The mechanisms of LRIC involve the regulation of the autonomic nervous system, the release of humoral factors, improvement of vascular endothelial function, and modulation of immune/inflammatory responses, which can antagonize the pathogenesis of hypertension through multiple pathways to lead to a drop in BP theoretically. This theory has been preliminarily confirmed by several small sample-size studies in non-resistant hypertension. This study aims to explore the efficacy and safety of remote ischemia adaptation for the treatment of resistant hypertension.

Interventions

DEVICERIC

RIC is a non-invasive therapy that is performed by automated pneumatic cuffs placed on bilateral arms. The RIC protocol includes five cycles of 5-min inflation to 200mmHg and 5-min deflation.

DEVICESham-RIC

The Sham-RIC protocol include five cycles of 5-min inflation to 60 mmHg and 5-min deflation by placing automated pneumatic cuffs on bilateral arms.

Sponsors

Ji Xunming,MD,PhD
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
30 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Aged 30\ 80 years old; * Taking ≥ 3 antihypertensive drugs (including one diuretic) for more than 4 weeks regularly; * Office blood pressure ≥ 140/90mmhg, and 24 h average blood pressure ≥ 130/80 mmHg; * Willing to participate in the study, follow the study protocol, and provide informed consent.

Exclusion criteria

* Secondary hypertension; * eGFR\<45ml/min/1.73m2; * Office blood pressure ≥180/110 mmHg, and 24 h average blood pressure ≥ 170/100 mmHg; * Hypertensive crisis occurred within 3 months; * Type 1 diabetes; * Cardiovascular events occurred within 3 months; * Atrial fibrillation; * Presence of any severe disease that adversely affects the subject or study; * Patients with contraindication for remote ischemic conditioning, such as vascular injury, soft tissue injury, orthopedic injury, or arm infection; * Pregnancy, lactation, or planned pregnancy; * Patients not suitable for this trial considered by researchers for other reasons; * Participation in another device or drug trial simultaneously.

Design outcomes

Primary

MeasureTime frameDescription
Changes of 24 h average systolic blood pressurefrom baseline to 8 weeksChanges of 24 h average systolic blood pressure from baseline to 8 weeks

Secondary

MeasureTime frameDescription
Changes of daytime average systolic blood pressurefrom baseline to 8 weeksChanges of daytime average systolic blood pressure from baseline to 8 weeks
Changes of daytime average diastolic blood pressurefrom baseline to 8 weeksChanges of daytime average diastolic blood pressure from baseline to 8 weeks
Changes of nighttime average systolic blood pressurefrom baseline to 8 weeksChanges of nighttime average systolic blood pressure from baseline to 8 weeks
Changes of nighttime average diastolic blood pressurefrom baseline to 8 weeksChanges of nighttime average diastolic blood pressure from baseline to 8 weeks
Changes of 24 h average diasolic blood pressurefrom baseline to 8 weeksChanges of 24 h average diasolic blood pressure from baseline to 8 weeks
Changes of office systolic blood pressurefrom baseline to 8 weeksChanges of office systolic blood pressure from baseline to 8 weeks
Changes of office diastolic blood pressurefrom baseline to 8 weeksChanges of office diastolic blood pressure from baseline to 8 weeks
Changes of home systolic blood pressurefrom baseline to 8 weeksChanges of home systolic blood pressure from baseline to 8 weeks
Changes of home diastolic blood pressurefrom baseline to 8 weeksChanges of home diastolic blood pressure from baseline to 8 weeks
Changes of 24 h average heart ratefrom baseline to 8 weeksChanges of 24 h average heart rate from baseline to 8 weeks

Contacts

Primary ContactXunming Ji, MD, PhD
jixm@ccmu.edu.cn83199430
Backup ContactWenting Guo
18368910464@163.com18368910464

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026