Clinical Trials Logo

Clinical Trial Summary

The investigators propose to adult patients needing the creation of a vascular access for hemodialysis, not eligible to the creation of a distal AVF, to create a percutaneous anastomosis between an artery and a vein (endo-AVFs). The study is a prospective single-center cohort (Nice University Hospital) with a 2-year follow-up (recruitment: 18 months, length of study per patient: 24 months, data analysis: 6 months). After the procedure, patients will receive duplex-ultrasound follow-up, according to local practice, at 6 weeks (+ surgical examination), 3, 6, 12, 18 and 24 months.


Clinical Trial Description

1. Inclusion baseline Visit The patient is adressed by his/her nephrologist for the creation of a vascular access for hemodialysis. It is provided with a venous and arterial map of the two upper limbs (not specific to the study) as well as a blood test necessary for anesthesia. 2. Inclusion visit The patient is examined by the vascular surgeon who determines, via arterial and venous mapping, and once the inclusion and non-inclusion criteria have been reviewed, whether he is eligible for the study. Participation in the protocol is then proposed to him. If he agrees to participate, the patient signs the informed consent after an appropriate time for reflection. The anesthesia consultation and the date of the procedure are scheduled during this visit. 3. Response: V0 The patient is hospitalized in the vascular surgery department, preferably in the day surgery unit, or in the full hospitalization department if he lives too far away or cannot be accompanied. Once in the operating room, and after anesthetic induction, the surgeon proceeds to create the percutaneous fistula. At the end of the intervention, the surgeon performs the shivering and the patient goes back to the service or remains for a while in the post-operative monitoring room depending on the anesthesia he has received. The patient is allowed to go home the same day for UCA patients, or the next day for patients on full hospitalization; once the surgeon has verified the presence of the thrill and the absence of signs of early ischemia, characterized or hematomas. The patient leaves with his appointment date at 6 weeks. 4. Follow-up to S6: V1 The patient is seen again 6 weeks after the operation. The consultation begins with a Doppler to determine: - Permeability of access - The absence of venous and arterial stenosis - The flow in the humeral artery - The internal diameter of the vein and artery 2cm from the anastomosis - Good distal hand perfusion The patient then sees the surgeon who proceeds: - The presence of thrill - The absence / presence of hematomas, lymphocele - Signs of venous hypertension - Signs of neurological deficit - Vascular steal syndrome This consultation (Doppler and surgical follow-up) is done routinely for all creations of fistulas and is not specific to the study. If the vascular access is ready to be used, the surgeon indicates the possible puncture points on the map obtained from the Doppler. The date of first dialysis is noted by the nephrologist. During the first 5 sessions, the nephrologist informs: The type of needle - Who performs the puncture - The use of ultrasonographic guidance to perform the puncture The nephrologist completes a satisfaction questionnaire at the end of the first dialysis session (as well as at 3, 6, 12, 18 and 24 months after the access was created). This questionnaire includes 5 items: ease of vein palpation, ease of vein puncture, appearance of the arm with respect to their prior experience, quality of dialysis and their overall satisfaction. 5. Monitoring at M3, M6, M12, M18 and M24: visits V2 to V6 The following visits contain a Doppler (identical to that carried out in V1 and included in the routine management of the patient) the results of which may lead to a consultation with the surgeon depending on the results. It is recommended that vascular access flow be measured monthly. The months without Doppler, it will be measured during dialysis sessions (according to Transonic or Dialysance depending on the equipment of the dialysis center). The frequency of the Dopplers will be adjusted if necessary in the event of reoperation and the opinion of the surgeon may be requested. ;


Study Design


NCT number NCT05897996
Study type Interventional
Source Centre Hospitalier Universitaire de Nice
Contact Nirvana SADAGHIANLOO
Phone 0492034702
Email causeret.m@chu-nice.fr
Status Not yet recruiting
Phase N/A
Start date July 1, 2024
Completion date December 1, 2025