Neuromuscular Electrostimulation in Radiocephalic Fistula (NCT02925845) | Clinical Trial Compass
UnknownNot Applicable
Neuromuscular Electrostimulation in Radiocephalic Fistula
Spain34 participantsStarted 2015-01
Plain-language summary
* Objective: To analyze the effect of neuromuscular electrostimulation in the maturation of radiocephalic arteriovenous fistula (RC-AVF) patients with chronic kidney disease (CKD) stage 5-5D
* Design: Clinical Trial with medical devices, 18-month, single-center, within the hospital setting.
* Disease or disorder study: vascular Access maturation.
* Population: Patients with CKD stage 5-5D at the research center.
* Project duration: 78 weeks
* Methodology:
* Patients with CKD stages 5-5D that has undergone a native AV in service stations to give their informed consent and meeting the inclusion criteria will be included.
* At baseline two study groups were established:
* Group 1: neuromuscular electrostimulation
* Group 2: isometric exercises
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
* Inclusion criteria:
* Patients aged less than 18 years old
* Patients with tracking CCEE Nephrology than 3 months
* Patients with AV native AV upper limb without prior
* Patients give their written informed consent
* Exclusion criteria:
* prior cardiovascular event (acute myocardial infarction, unstable angina, stroke ....) in the last 3 months.
* AV prior to HD in same upper extremity
* Not have given informed written consent
* Carrier cardiac pacemaker
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Radiocephalic fístula flow ( millimeters/minuts)
Timeframe: 8 weeks ultrasonography parameter of maturation