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External application of Tongmai Xiaotong prescription combined with stone needle ironing on autogenous arteriovenous fistula Protective effect and its mechanism exploration

External application of Tongmai Xiaotong prescription combined with stone needle ironing on autogenous arteriovenous fistula Protective effect and its mechanism exploration

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000547
Enrollment
Unknown
Registered
2024-10-14
Start date
2024-11-10
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Hemodialysis autologous arteriovenous fistula in chronic kidney disease

Interventions

A group:The first stage ( 1-12 weeks ) : Tongmai Xiaotong Decoction combined with stone ironing treatment
elution period ( 13-16 weeks ) : routine maintenance, dynamic information monitoring
the second stage ( 17-28 weeks ) : routine maintenance, dynamic information monitoring, non-intervention
B group:The first stage ( 1-12 weeks ) : routine maintenance, dynamic information monitoring, non-intervention
the second stage ( 17-28 weeks ) : Tongmai Xiaotong Decoction combined with stone ironing treatment.

Sponsors

Department of Nephrology, Xiyuan Hospital, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? 1ESRD patients with regular hemodialysis = 3 months and stable condition ; ? 2 Patients aged 30-80 years old regardless of gender ? 3 Patients who were treated with AVF for dialysis each time which met the criteria for judging the maturity of AVF in the consensus of Chinese experts on vascular access for dialysis : good anastomotic tremor no abnormal enhancement weakening or disappearance straight fistula vein superficial easy to puncture uniform thickness and sufficient puncture area. The natural blood flow was > 500 ml / min the inner diameter of the puncture vein was = 5 mm and the depth from the skin was < 6 mm. ? 4 The dialysis program was regular hemodialysis 3 times a week and the arteriovenous puncture needles were 16 G and 17 G ; ? 5 The pump-controlled blood flow was 200-260 ml / min. ? 6 Volunteered to participate in the experiment and signed the informed consent.

Exclusion criteria

Exclusion criteria: ? 1 patients with drug allergy and intolerance of treatment technology in the prescription ; ? 2 patients with open skin damage or skin lesions in the treatment area ; ? 3 patients with arteriovenous fistula blood flow dysfunction ( stenosis, thrombosis, etc. ) or other serious complications requiring intervention ; ? 4 Unstable vital signs, or combined with a variety of important organ failure and immune diseases, as well as other serious systemic diseases, such as cirrhosis, blood system diseases and malignant tumors ; patients with bleeding tendency diseases ; ? 5 is participating in other clinical researchers.

Design outcomes

Primary

MeasureTime frame
Ultrasonic index;

Secondary

MeasureTime frame
fistula patency rate;Puncture pain assessment;rate of complications;High-sensitivity C-reactive protein, interleukin-6, vascular endothelial factor;

Countries

China

Contacts

Public ContactLin-yang Li

Xiyuan Hospital of China Academy of Chinese Medical Sciences

linyanglilia@163.com13811330822

Outcome results

None listed

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