Clinical Trials Logo

Clinical Trial Summary

This study will compare the outcomes of tunneled femoral catheter and femoro-femoral arteriovenous graft as a bailout procedure for hemodialysis in chronic kidney disease patients with exhausted upper-extremity and chest-wall vascular accesses regarding survival rate, complications, and quality of life


Clinical Trial Description

Aim of the Work: The aim of this work is to compare the outcomes of tunneled femoral catheter (TFC) and femoro-femoral AVG as regards survival, complication and quality of life as bailout procedure for hemodialysis in CRF patient with exhausted upper limb extremity and chest wall vascular accesses. Patients and Methods: Study Design and setting: This is a single-centre prospective randomized controlled trial that will be conducted in The Vascular Surgery Department, Mansoura University Hospital, during the period from November 2020 to November 2022. It will be submitted for approval by Institutional Review Board, faculty of medicine, Mansoura University. Eligibility criteria: The study population will be on patients referred to the vascular surgery department suffering from end-stage renal disease (ESRD) with exhausted upper-extremity and chest wall vascular accesses. Inclusion: In this study, The investigator will include all ESRD patients belonging to the age group (≥ 15 years) who complain of exhaustion of all upper extremity vascular accesses. Exclusion: The investigators will exclude patients with previous history or evident deep venous thrombosis (DVT), varicose veins, femoral vein stenosis, arterial insufficiency, severe groin or limb infection. Preoperative assessment: A comprehensive history will be taken from the patients with regard to patient's demographics, underlying medical conditions, duration since the starting of haemodialysis, previous trials of vascular access, history of DVT and arterial insufficiency. Also, patients will be examined to exclude any possibility for upper extremity vascular access. A meticulous examination of both lower limbs is done to assess the possibility of infection, signs of venous stenosis or arterial inefficiency including palpation of accessible lower limb arteries. Routine laboratory investigations are carried out for all patients including complete blood count, liver function tests, renal function tests, arterial blood gases, bleeding and coagulation profiles, fasting and 2hr-postprandial serum glucose level, lipid profile, and glycosylated hemoglobin (HbA1c). Further investigations include duplex ultrasonography (US) assessing for both superficial and deep venous system of the both lower limb. Bilateral lower limb arterial duplex is done to exclude any arterial disease. Also, a preoperative venous mapping of lower limb veins is mandatory. Procedures and Postoperative care: Procedures: 1. Tunneled femoral catheter: a standard technique is adopted according to the study performed by Herzallah using long tunneled catheter. 2. Femoral artery-femoral arteriovenous graft: a straight or loop configuration Ponikvar Endpoints and Follow-up: Every patient will be followed every week until first month, then every 3 months until the end of the first years so that the hemodynamic improvement will be assessed. Primary outcome: • Evaluation of primary patency rates within the study follow-up time frame. - In case of TFC: Normally an extracorporeal blood flow should be about 300 ml/min. based on this, the catheter dysfunction can be defined by the first occurrence of either peak blood flow of 200 ml per minute or less for 30 minutes during a dialysis treatment, mean blood flow of 250 ml per minute or less during two consecutive dialysis treatments, or inability to initiate dialysis owing to inadequate blood flow, after attempts to restore patency have been attempted. - In case of AVG, stenosis > 50% of the prosthesis diameter or complete occlusion is considered significant. This can be assessed by duplex ultrasonography every six months or when the patency is questionable. The patency rates will be determined according to the reporting standards, set by the Committee of Reporting Standards for arteriovenous hemodialysis accesses Secondary outcome: - The secondary patency: the patency rates will be determined according to the reporting standards, set by the Committee of Reporting Standards for arteriovenous hemodialysis accesses - The special adverse events complicating lower-extremity hemodialysis access. The severity of arteriovenous access complications will be graded according to the Reporting Standards document . Complications are defined according Clavien-Dindo. - Patient satisfaction will be assessed using a validated tool, the vascular access score questionnaire, at 6 and 12 months postoperatively. - Besides, operative time, hospital stay, and survival rate will be assessed. Sample size calculation: Based on the average of the primary outcome (primary patency), a previous study showed that the mean rate in AVGs at 6 months was 53%, while another study showed that the mean rate in TFC at six months was 14%. Using sample size calculation software (www.clincalc.com), a minimum of 44 patients will be needed to achieve a study power of 80% with alpha set at 5%. Estimating a drop-out rate and loss to follow-up of 10%, a total of 48 patients will be ultimately included. Random sequence generation and blinding: Patients will be randomized to one of two groups; group I Tunneled femoral catheter and group II Femoral artery-femoral vein graft. Randomization will be undertaken by the sealed envelope method using randomization software. Neither the operating surgeons nor the assessors during the follow-up will be aware about patients' participation in the study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04746742
Study type Interventional
Source Mansoura University
Contact Mohammed Mosallam M Ibrahim, Specialist of Vascular Surgery
Phone 01001518995
Email mohammedmosallam90@gmail.com
Status Recruiting
Phase N/A
Start date December 1, 2020
Completion date December 1, 2022

See also
  Status Clinical Trial Phase
Withdrawn NCT04136561 - Novel Strategy to Encourage Early Removal of Central Venous Catheters N/A
Active, not recruiting NCT04054128 - Bicarbonate vs Heparin Catheter Lock in Chronic Hemodialysis Patients Phase 4
Completed NCT02297308 - A Retrospective Study Evaluating the Use of the SoloPath® Sheath in Reducing Vascular and Bleeding Complications N/A
Completed NCT01446263 - RADIAL Versus Femoral Access for Coronary Artery Bypass Graft Angiography and Intervention (RADIAL-CABG) Trial Phase 3
Recruiting NCT05132712 - Effects of Angiotensin Converting Enzyme Inhibitors on Patency of Arterio-Venous Fistulas: A Randomized Controlled Trial Early Phase 1
Completed NCT02513303 - Trial to Evaluate the Sirolimus-Eluting Collagen Implant on AV Fistula Outcomes Phase 3
Completed NCT02200458 - Near-infrared Software Performance Study N/A
Recruiting NCT06001827 - SAVE-FistulaS: the SelfWrap-Assisted ArterioVEnous Fistulas Study N/A
Recruiting NCT04077762 - Radial vs. State-Of-The-Art Femoral Access for Bleeding and Access Site Complication Reduction in Cardiac Catheterization (REBIRTH) N/A
Completed NCT05982366 - Feasibility and Safety of the Routine Distal Transradial Approach N/A
Completed NCT05101720 - Ultrasound Guided Axillary Access vs Standard Fluoroscopic Technique for Cardiac Lead Implantation: ZEROFLUOROAXI TRIAL N/A
Terminated NCT03879824 - Radial Versus Femoral Secondary Access During TAVI N/A
Recruiting NCT05741866 - Novel Antimicrobial Dressing in Peripheral Intravenous Catheters (PIVCs) N/A
Completed NCT05093699 - Dual-plane Ultrasound Imaging During Vascular Access Procedures N/A
Recruiting NCT02449798 - Prospective Feasibility Trial of AccuCath 2.25" BC Placed in Difficult Access Patients in the Emergency Department N/A
Active, not recruiting NCT02808208 - Autologous Adipose Derived Mesenchymal Stem Cells (AMSC) in Reducing Hemodialysis Arteriovenous Fistula Failure Phase 1/Phase 2
Completed NCT04409418 - Blood Sampling Functionality of Extended Dwell Catheters N/A
Recruiting NCT04472221 - Arterio-arterial Vascular Access as a Novel Technique for Treatment of Venous Hypertention With Arterio-venous Vascular Access N/A
Completed NCT02558153 - RCT of Paclitaxel DEB Compared to Standard PTA in Dialysis Fistula N/A
Completed NCT01927185 - Long-versus Short-Axis Ultrasound Guidance for Subclavian Vein Cannulation N/A