Comparison of Effectiveness and Complications of Catheter Lock Solutions in Non-tunneled Hemodialysis Catheters

Sponsor
Zonguldak Ataturk State Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT04772209
Collaborator
Cumhuriyet University (Other), Sisli Hamidiye Etfal Training and Research Hospital (Other)
400
3
2
22.9
133.3
5.8

Study Details

Study Description

Brief Summary

In our study, investigators will investigate the effectiveness and complications of two catheter lock solutions one of which is the standard heparin routinely used in comparison to Sodium bicarbonate. Both solutions were used but not compared head to head. Investigators aim to compare both solutions in terms of catheter lumen patency and their effect on catheter-related infections.

Detailed Description

The most important problem in patients with end-stage renal disease or patients with acute renal failure needing urgent hemodialysis treatment is the lack of appropriate vascular access. In acute situations, vascular access is usually provided by non-tunneled catheters. Main problems with this temporaray vascular access is failure due to lumen thrombosis. anther major problem is catheter related infection. In some patients, there is a handicap of using heparin. In some situations, heparin is not preferred for use. In terms of the probable shortage of resources and cost-effectiveness, Investigators aimed to compare head to head the superiority and non-inferiority of each solution. Sodium bicarbonate was compared to the isotonic solution and found to be effective for a short time. The main aim of this study is to compare both classic Heparin and sodium bicarbonate in Femoral and Jugular catheters aimed for dialysis. In both arms, the maximum patency and the observed side effects will be recorded. The maximal time used will be recorded. statistical analysis will be planned to compare the two groups.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
400 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Bicarbonate vs Heparin group (femoral vs jugular catheter)Bicarbonate vs Heparin group (femoral vs jugular catheter)
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Comparison of Effectiveness and Complications of Heparin and Sodium Bicarbonate Catheter Lock Solutions in Non-Tunneled Hemodialysis Catheters
Actual Study Start Date :
Feb 1, 2021
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Dec 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Sodium bicarbonate Arm

In this arm, the catheter lock solution is sodium bicarbonate

Drug: Sodium bicarbonate
Dialysis catheter lumen will be filled (locked) by sodium bicarbonate solution. The amount of solution depends on the diameter and length and will be in accordance with the manufacturer's specifications.

Active Comparator: Heparin arm

In this arm, classic heparin will be used as a reference catheter lock solution (standard lock solution)

Drug: Heparin
Dialysis catheter lumen will be filled (locked) by classic heparin. The amount of pure heparin depends on the diameter and length and will be in accordance with the manufacturer's specifications.

Outcome Measures

Primary Outcome Measures

  1. Time to first catheter failure (day) [6 months]

    The time from first sucessful dialysis session to the last one (in days)

  2. Total Duration of catheter usage (day) [6 months]

    some patients need only 1-2 dialysis sessions while others may need too many sessions. In some cases a total of three dialysi sessions is whithin 3-4 days while others may need that number in wider range (e.g 10-14 days). Here both number and duraion effect is evaluated

  3. Number of participants with catheter occlusion [6 months]

    The number of cases early catheter

  4. Number of patients with catheter related infection [6 months]

    any catheter related infection(exit site, lumen inection etc) will be recorded

  5. Time of catheter occlusion or failure [6 months]

    catheteres occluded by thrombi will be documented

  6. Causes of premature catheter malfunction [6 months]

    any catheter needing exchange prematurly will be be evaluated for mulfunction cause (etiher mechanical thromus or kink rtc.)

Secondary Outcome Measures

  1. Total number of dialysis sessions with active patent catheter usage [6 months]

    In some cases intensive treatment is indicated. the effect of frequent usage of catheteres will be evaluated

  2. Number of cases with venous thrombosis [6 months]

    catheters especially femoral have a risk of venous thrombosis, any clincal sign of thrombosis will be recorded. In case of catheter removal doppler ultrasound will be documented.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 100 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • All patients over 18 years who assign consent will be included
Exclusion Criteria:
  • patients less than 18 years of age

  • Patients with active arterial or venous thrombosis problems

  • Thrombocytopenic patients

  • Patients with hypercoagulable states

  • Patients with contraindications to heparin usage

Contacts and Locations

Locations

Site City State Country Postal Code
1 Şişli Etfal State Hospital Istanbul TN Turkey 34362
2 Cumhuriyet University Hospital Sivas TN Turkey 34762
3 Zonguldak ataturk state hospital Zonguldak TN Turkey 67100

Sponsors and Collaborators

  • Zonguldak Ataturk State Hospital
  • Cumhuriyet University
  • Sisli Hamidiye Etfal Training and Research Hospital

Investigators

  • Principal Investigator: MAHMUD M ISLAM, MD, Zonguldak Ataturk State Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
mahmud islam, Medical Director of Nephrology clinic, Zonguldak Ataturk State Hospital
ClinicalTrials.gov Identifier:
NCT04772209
Other Study ID Numbers:
  • ZADH-1
First Posted:
Feb 26, 2021
Last Update Posted:
Feb 8, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by mahmud islam, Medical Director of Nephrology clinic, Zonguldak Ataturk State Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 8, 2022