Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2025-12-25 @ 4:06 AM
Ignite Modification Date:
2025-12-25 @ 4:06 AM
NCT ID:
NCT03645720
Brief Summary:
The purpose of this study is to evaluate the complication of the puncture related complication in AVG (arteriovenous graft) such as pseudoaneurysm and hematoma, and the dialysis adequacy using plastic cannula versus metal needle in hemodialysis patients
Detailed Description:
1. Ultrasonography is performed to determine the maturity of vascular access 4 weeks after AVG creation.
2. The first puncture is performed with plastic cannula or metal needle when it is judged that the blood vessel has matured.
3. Four skilled nurses perform vascular access puncture with plastic or metal needle
4. Ultrasound are used to evaluate and record the complications related to the puncture in plastic or metal needle group every month.
5. Complications and dialysis adequacy between the two groups will be evaluated after 6 months
Study:
NCT03645720
Study Brief:
Protocol Section:
NCT03645720