Arteriovenous Fistula Clinical Trial
Official title:
Neuromuscular Electrostimulation Effect on the Maturation of Native Vascular Access (VA) Patients With Kidney Disease 5- Chronic Stages 5d Estimated by Doppler Ultrasound
- 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
- 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
- At baseline, patients included in the study the main demographic variables were
collected, anthropometric, biochemical parameters, hemodynamic data, Eco Doppler of AV
(ECO mapping) and prescribed medical treatment.
- Likewise, they will be made an assessment of their muscle strength by skinfold and
upper limb static dynamometry in which was made the native AV.
- During the study period the following phases were established:
• Phase 1 (4 weeks):
- The control group will receive the usual care on an outpatient AV.
- Patients assigned to group, will perform a program of AV electrostimulation in the
affected upper extremity (according to program) after 7 days of completion of native
AV.
- At the end of this phase both groups were conducted an ECO doppler (ECO4s) AV regulated
by Vascular Surgery.
• Phase 2 (8 weeks):
- The control group will receive the usual care on an outpatient AV.
- Patients assigned to group, will perform a program of AV electrostimulation in the
affected upper extremity (according to program)
- At the end of this phase, both groups were conducted an ECO doppler (ECO8s) is
regulated by the AV Vascular Surgery
- During all phases of the study, patients on hemodialysis follow their analytical
controls programmed by Nephrology and receive medical treatment according to standard
clinical practice.
- At the end of each phase of the study, all patients were performed an assessment of
their muscle strength by centimetría, skinfold thickness and static dynamometry member
in which AV has been made.
- Calendar: A provisional timetable is presented
- Presentation of the CEIC study: September 2014
- inclusion Period: 78 weeks
- Follow-up period: 2 months
- Close database: 1 month
- Statistical analysis: 1 month
- Source of funding: Not available
;
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05302505 -
Simulation-based Training for Nurses and Arteriovenous Fistula Puncture in Chronic Hemodialysis Patients
|
N/A | |
Terminated |
NCT01642459 -
The Outcomes of Arteriovenous Fistula Cannulated From Different Direction.
|
N/A | |
Recruiting |
NCT04017806 -
Investigating the Role of Luminal Pressure on Arteriovenous Fistula Maturation
|
||
Terminated |
NCT03668002 -
Trial of Fistula Versus Graft in Elderly Patients
|
N/A | |
Completed |
NCT06199609 -
Changes in Cardiac Structure and Function After Establishment of Autologous Arteriovenous Fistula
|
||
Recruiting |
NCT04034433 -
Exercise Program for Arteriovenous Fistula Maturation
|
N/A | |
Active, not recruiting |
NCT04629118 -
Intervention With Selution SLR™ Agent Balloon for Endovascular Latent Limus Therapy for Failing AV Fistulas (ISABELLA) Trial
|
||
Recruiting |
NCT02913365 -
Etiologies, Investigations and Outcomes of Patients Presenting With Hemoptysis
|
N/A | |
Recruiting |
NCT05616104 -
FLEX FIRST Registry Research Protocol
|
||
Recruiting |
NCT03886116 -
Effect of Pre-operative Forearm Exercises on Arterial Venous Fistula Maturation and Blood Flow
|
N/A | |
Completed |
NCT02513303 -
Trial to Evaluate the Sirolimus-Eluting Collagen Implant on AV Fistula Outcomes
|
Phase 3 | |
Completed |
NCT01863914 -
Vascular Protective Effect of Rosuvastatin in Arteriovenous Fistula
|
Phase 2 | |
Recruiting |
NCT06001827 -
SAVE-FistulaS: the SelfWrap-Assisted ArterioVEnous Fistulas Study
|
N/A | |
Recruiting |
NCT04543539 -
IN.PACT™ AV Access Post-Approval Study (PAS002)
|
||
Completed |
NCT05326321 -
Effect of Virtual Reality Glasses in The Arteriovenous Fistule Cannulation Processon Paın and Patient Satisfaction
|
N/A | |
Recruiting |
NCT03741985 -
Effect of Dumbbell Exercise on Arteriovenous Fistula in Patients With Hemodialysis
|
N/A | |
Terminated |
NCT03566927 -
FLEX®-DCB Dialysis ACCESS Stenosis Study
|
N/A | |
Not yet recruiting |
NCT04393688 -
Study Evaluating the Safety and Efficacy of Tri-wire Balloon for Treatment of Dysfunctional AV Fistula
|
N/A | |
Recruiting |
NCT02447796 -
Dexmedetomidine and Propofol As Sole Sedative Agent for Patients Undergoing Arteriovenous Fistula Surgery
|
Phase 4 | |
Terminated |
NCT01321866 -
Cutting Balloon Versus Non-cutting Balloon for the Treatment of Venous Stenosis in the Fistulas of Hemodialyzed Patients
|
N/A |