Condition: Arteriovenous Graft Stenosis · Sponsor: DK Medical Technology (Suzhou) Co., Ltd.
This is a multicenter, prospective, randomized controlled clinical study. Patients with hemodialysis arteriovenous graft fistula stenosis will be recruited to explore whether the scoring balloon is superior to the high pressure balloon in treating such lesions, so as to provide a basis for optimizing the treatment of such lesions. This study will be conducted in seven (7) clinical trial institutions, with a total of 140 subjects included. After randomization, the subjects will use either the scoring balloon dilatation catheter, developed and produced by DK Medical Technology Co., Ltd., or the peripheral balloon dilatation catheter for surgical treatment. Clinical follow-up will be carried out within 5 days, 3 months, 6 months, and 12 months after the procedure.
This description comes directly from the study's public registry record.
Pei Wang, MD · +86 13523467291 · wangpei146@hotmail.com
Always discuss trial participation with your own doctor first.
| Beijing Tongren Hospital Affiliated to Capital Medical University | Beijing, Beijing Municipality, China | Not Yet Recruiting |
| Guangdong Provincial People's Hospital | Guangzhou, Guangdong, China | Not Yet Recruiting |
| South China Hospital of Shenzhen University | Shenzhen, Guangdong, China | Not Yet Recruiting |
| The First Affiliated Hospital of Zhengzhou University | Zhengzhou, Henan, China | Not Yet Recruiting |
| The Second Affiliated Hospital of Nanjing Medical University | Nanjing, Jiangsu, China | Not Yet Recruiting |
| Longhua Hospital Affiliated to Shanghai University of Traditional Chinese Medicine | Shanghai, Shanghai Municipality, China | Recruiting |
| National University Hospital of Singapore | Singapore, Singapore | Not Yet Recruiting |
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Source record: clinicaltrials.gov/study/NCT06503692