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To Investigate the Effect of Far-infrared Radiation on Lower Extremity Acupoints on the Blood Circulation of Lower Extremities in Patients With Hemodialysis

To Investigate the Effect of Far-infrared Radiation on Lower Extremity Acupoints on the Blood Circulation of Lower Extremities in Patients With Hemodialysis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05822960
Enrollment
32
Registered
2023-04-21
Start date
2023-02-20
Completion date
2023-08-10
Last updated
2023-11-22

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

Conditions

Peripheral Arterial Disease

Keywords

hemodialysis, peripheral arterial occlusion disease, far-infrared radiation, lower extremity acupoints, ankle-brachial index, Edinburgh claudication questionnair

Brief summary

This study intends to irradiate the acupoints of both lower extremities of hemodialysis patients with far-infrared therapeutic apparatus to explore its effect on foot blood circulation, peripheral artery occlusion disease (PAOD) symptoms and ankle-brachial index (Ankle-Brachial Index, ABI) value.

Detailed description

After irradiating the lower extremity acupoints of hemodialysis patients with far-infrared rays, it is expected to improve the blood circulation of the lower extremities of hemodialysis patients, thereby improving the symptoms of indirect claudication and raising the ankle-brachial index to the normal range, and reducing the incidence of peripheral arterial disease in hemodialysis patients. The results of this study can provide an empirical reference for future clinical care.

Interventions

DEVICEfar-infrared radiation

far-infrared radiation on foot acupoints (Yinlingquan and Sanyinjiao acupoints) during dialysis

Sponsors

Chung Shan Medical University
CollaboratorOTHER
National Taiwan University Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

The dialysis day was W 1.3.5 as the control group and W 2.4.6 as the experimental group.

Eligibility

Sex/Gender
ALL
Age
25 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* 1.Patients diagnosed with chronic renal failure in a hemodialysis unit and receiving hemodialysis for at least three months 2. Willing to participate in interventional treatment with far-infrared radiation 3. Willingness to cooperate with intervention measures and inspection time 4. Receive hemodialysis treatment three times a week

Exclusion criteria

1. There are contraindications for ABI examination (such as breast cancer lymph node dissection in the past), bilateral upper limb arteriovenous access, etc.), and a double- lumen dialysis venous catheter is placed in the groin 2. Bedridden or unable to walk 3. History of distal amputation, DVT, CABG s/p due to trauma, ischemia or infection 4. Consciously unclear and unable to cooperate 5. Patients with wounds from calf to instep

Design outcomes

Primary

MeasureTime frameDescription
Comparison of the Edinburgh Claudication Questionnaire and ABI after receiving far-infrared lower extremity acupoint irradiation therapy (investigators ) and general clinical care (participants) change assessedintervention 1,2,3 and 6 month change is being assessedinvestigators :receiving far-infrared intervention;participants :general clinical care

Secondary

MeasureTime frameDescription
Comparison of basic data and disease characteristics distribution between the two groupstwo groups before receiving far-infrared intervention (month 0)change is being assessedDemographic characteristics include: gender(boy or gril), age, education level, smoking history, presence/absence of exercise, and drinking; disease characteristics include(yes or no): years of dialysis(year), presence/absence of anticoagulant drugs(yes or no); disease history(yes or no): diabetes, hypertension, coronary artery disease disease, cerebrovascular disease The monthly routine inspection items in the hemodialysis room are designed,
To compare the Edinburgh claudication questionnaire and ABI before (month 0) receiving far-infrared lower extremity acupoint irradiation therapy and general clinical caretwo groups before receiving far-infrared intervention (month 0)change is being assessed,In this study, used the Chinese version of the Edinburgh Claudication Questionnaire as a screening test for intermittent claudication symptoms; This study intends to use ABI-type equipment for measurement. Because hemodialysis patients have the limitation that the arm on the side of the arteriovenous fistula can not measure blood pressure, the modification is as follows Calculation method: ABI of left foot = systolic pressure of left posterior tibia ÷ systolic pressure of brachial artery without arteriovenous fistula;ABI of right foot is also calculated in the same way

Countries

Taiwan

Outcome results

None listed

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