Taurolock Hep 500 Versus Unfractionated Heparin as Anti-inflammatory in Hemodialysis Catheters.

Sponsor
Ain Shams University (Other)
Overall Status
Unknown status
CT.gov ID
NCT03539718
Collaborator
(none)
60
1
2
8.6
7

Study Details

Study Description

Brief Summary

To assess the efficacy of Taurolock-hep500™ as anticoagulant and antimicrobial catheter lock solution in comparison to unfractionated heparin as alock solution to improve performance of hemodialysis catheters and quality of hemodialysis .

Condition or Disease Intervention/Treatment Phase
  • Drug: Taurolidine heparin
  • Drug: Heparin Sodium
Phase 4

Detailed Description

In this study,investigators will recruit 60 patients with ESRD on regular hemodialysis from hemodialysis units in Ain-Shams university Hospitals, Patients will be recruited to study at the time of catheter insertion.

They will be randomized into 2 groups. Group 1; 30 Patients will receive unfractionated heparin (5000i.u/ml) after hemodialysis sessions (control group).

Group 2; 30 Patients will receive Taurolock-hep500™ after hemodialysis sessions. All patients will be subjected to;

  1. Full history including history of ESRD and dialysis initiation.

  2. Clinical examination. Aseptic technique will be used in handling with catheters including (sterile gloves, antiseptic solution in dealing with covers and caps topical antibiotics spray and ointment) catheter will be instilled by 10 ml of normal saline in both opening followed by either taurolock hep 500™ or unfractionated heparin 5000 iu/ml.

Patients will be followed up for one month and will be monitored for clinical symptoms and signs of catheter related bacteremia (fever ,rigors, hypotension, sweating ) on the hemodialysis sessions . Also catheter performance will be assessed using the following parameters;

  1. Blood flow rate measured by hemodialysis machine blood pump in (ml/min).

  2. Dialysis quality by URR( urea reduction ratio) is a dimensionless number used to quantify dialysis treatment adequacy by calculating difference between urea level before and after hemodialysis session (average of 4 sessions , 1 per each week).

  3. CBC ,markers of inflammation (CRP) baseline and at time of appearance of symptoms and signs of bacteremia in both groups in addition to (IL6) measured by Elisa technique baseline and at time of appearance of symptoms and signs .

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
comparativecomparative
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Taurolidine Citrate and Unfractionated Heparin Combination Versus Unfractionated Heparin Alone in Prevention of Inflammation in Hemodialysis Catheters.
Actual Study Start Date :
May 15, 2018
Anticipated Primary Completion Date :
Nov 1, 2018
Anticipated Study Completion Date :
Feb 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: cases

Cases, taurolidine heparin 500 will be used at end of session

Drug: Taurolidine heparin
Taurolock-hep 500 at end of session
Other Names:
  • Tautolock HEP 500
  • Active Comparator: control

    Controls, Heparin Sodium 5000 will be given at end of session

    Drug: Heparin Sodium
    Heparin sodium 5000 at end of session
    Other Names:
  • Heparin Sodium 5000
  • Outcome Measures

    Primary Outcome Measures

    1. Prevention of inflammation in hemodialysis patients through hemodialysis catheters [one month]

      Comparing levels of highly sensitive c-reactive protein and interleukin-6 levels before and after using the drug Urea reduction ratio over sessions

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Patients on regular hemodialysis 3sessions/wk.

    2. Recent catheter insertion at beginning of the study.

    3. Both males and females.

    4. Age group ≥ 18 ys.

    Exclusion Criteria:
    1. Patients with intercurrent infections.

    2. Patients with sepsis.

    3. Patients receiving drugs affecting immune system like immunosuppressive drugs.

    4. Patients on antibiotics.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Ain Shams University Hospitals Cairo Egypt 002

    Sponsors and Collaborators

    • Ain Shams University

    Investigators

    • Study Director: Magdy Sharkawy, MD, Ain Shams University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    amr mohamed mansour, Assistant Lecturer of nephrology, Ain Shams University
    ClinicalTrials.gov Identifier:
    NCT03539718
    Other Study ID Numbers:
    • taurolock hep 500 efficacy
    First Posted:
    May 29, 2018
    Last Update Posted:
    May 29, 2018
    Last Verified:
    May 1, 2018
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 29, 2018