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??? Evaluation of the effect of using autologous saphenous vein as a hemodialysis alternative access in hemodialysis-dependent ESRF patient

Evaluation of the effect of using autologous saphenous vein as a hemodialysis alternative access in hemodialysis-dependent ESRF patient

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240911063008N1
Enrollment
28
Registered
2024-10-09
Start date
2024-10-31
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Evaluation of the effect of using autologous saphenous vein as a hemodialysis alternative access in hemodialysis-dependent ESRF patient.

Interventions

Intervention group: All ESRF patients who do not have adequate vascular access in their autologous vein and are candidates to be placed in the artificial vein method group..

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients with ESRD

Exclusion criteria

Exclusion criteria: ???????? ?? ?? ?? ????? ????? ?????? ???? ????? ??? ???? ? ?????? ?? ?????? ????? ??????? ?? ??? ???? ????? ? ??? ???? ??? ??? ???? ?? ???? ?? ?????? ??? ????? ?? ??? ?????

Design outcomes

Primary

MeasureTime frame
Primary:Operative failure rate, 1-year patency rate, venous occlusion. Secondary: infection, cannulation, ischemia of blood vessels, aneurysm, seroma leakage. Timepoint: Patients will be evaluated at four time points (before and immediately after surgery, six weeks and three months after surgery). Method of measurement: In this study, permutation blocks method was used to generate the sequence of random assignment of people to the studied groups. The sequence of random allocation of people was done using Random Allocation Software and the block size was four. The permutation block method is one of the random allocation methods in which each block is selected according to the number of studied groups. In this study, six blocks AABB (1), ABAB (2), ABBA (3), BBAA (4) ), BABA (5) and BAAB (6). One of the blocks is randomly selected. If the first block, AABB, is selected, the first and second people are assigned to group A, and the third and fourth people are assigned to group B, and this process continues until all the samples are assigned. The characteristic of this method is that the two study groups will have equal numbers.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoud Ostadi sefidan

Mashhad University of Medical Sciences

Masoud.6813@yahoo.com+98 51 3804 0000

Outcome results

None listed

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