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Management of Tunneled Catheter Thrombosis in Hemodialysis Patients: Prospective Study From Qatar

Primary Purpose

Hemodialysis, Tunneled Catheter, Qatar

Status
Completed
Phase
Phase 4
Locations
Qatar
Study Type
Interventional
Intervention
TauroLock U 25000
(TauroLock Hep500)
Sponsored by
Hamad Medical Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hemodialysis, Tunneled Catheter, Qatar

Eligibility Criteria

14 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 1- Adult patients aged>14 years 2- Undergoing HD through tunneled HD 3- Recently inserted or old tunneled catheter 4- Blood flow rate at the beginning of the study≥ 300ml/min

Exclusion Criteria:

  • 1- Malfunctioning catheter defined by blood flow rate < 300ml/min 2- Known patient to have allergy to drug medication 3- Major Hemorrhage in previous 4 week

Sites / Locations

  • Fahd Bin Jassem Dialysis Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

A

B

Arm Description

We will lock the dialysis catheter post HD with TauroLock Hep500 at the end of of all Hemodialysis sessions and during all interdialytic periods

We will lock the dialysis catheter post HD with TauroLock Hep500 at the end of the first two session only per week and during first two interdialytic periods then TauroLock U 25000at the end of third session before week end, (over the week end).

Outcomes

Primary Outcome Measures

Number of catheter thrombosis episodes
The time to first episode of catheter thrombosis lead to catheter change. Number of acute episode of thrombosis that interrupt dialysis Median Survival life of the catheter in both groups after adjusting it to the outcome.

Secondary Outcome Measures

Amount of r-TPA used in each group for treatment of acute catheter thrombosis
as above
Number of catheter exchange in each group
Hospitalization days related to catheter malfunctioning or CRI in each group

Full Information

First Posted
June 28, 2016
Last Updated
August 14, 2016
Sponsor
Hamad Medical Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT02868697
Brief Title
Management of Tunneled Catheter Thrombosis in Hemodialysis Patients: Prospective Study From Qatar
Official Title
Management of Tunneled Catheter Thrombosis in Hemodialysis Patients: Prospective Study From Qatar
Study Type
Interventional

2. Study Status

Record Verification Date
June 2016
Overall Recruitment Status
Completed
Study Start Date
November 2013 (undefined)
Primary Completion Date
August 2015 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hamad Medical Corporation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Goal of the study: A- To find out the best protocol for catheter lock solution to decrease the prevalence of catheter thrombosis - The time to first episode of catheter thrombosis lead to catheter change. - Number of acute episode of thrombosis that interrupt dialysis - Median Survival life of the catheter in both groups after adjusting it to the outcome. B- Specific Objective: To evaluate the cost effectiveness by measure 1- Amount of r-TPA used in each group to treatment acute catheter thrombosis 2- Number of catheter exchange in both group 3- Hospitalization days related to catheter malfunctioning or CRI in each group 4- Type and days of antibiotics 5- Cost of the treatment in each group c- Secondary Objective: To correlate the result of two catheters lock solution protocols with the published data using r-TPA instead of heparin once week as compared with heparin 3 times per week as a locking solution.
Detailed Description
This prospective single blind randomized controlled study. All patients who undergoing tunneled catheter regular hemodialysis in the three hemodialysis units and meet the inclusion criteria will be included in the study. Signed informed consent will be taken from all patients or their first authorized relative. All patients will be randomized on 1:1 basis using computer-generated program.Patients will be randomly assigned to lock the catheter post HD either with 1.35% taurolidine citrate (2H-1,2,4-thiadiazine-4,4'-methylenebis[tetrahydro-1,1,1',1'-tetraoxide], 4% citrate and 500 IU/ml heparin (TauroLock Hep500) (TauroPharmGmbH, www.tauropharm.de) at the end of of all Hemodialysis sessions and during all interdialytic periods or after the first two session only per week and during first two interdialytic periods then taurolidine citrate, 4% citrate /25000 IU unit urokinase (TauroLock U25000) at the end of third session before week end, (over the week end). The assigned nurse will flush the catheter after each session with 20 mL of saline then instill TauroLock according to the filling volume of the catheter. Before starting the next dialysis the lock solution has to be aspirated and discarded. Acute catheter thrombosis which interrupt the dialysis will be treated with r-TPA according to unit protocol, if this happen for three consecutive HD we will consider it as malfunction and we will refer it for catheter exchange . Any catheter will be referred to the vascular surgeon for exchange; we will not continue calculating its days as there might be a gap between referral's time and catheter exchange due admission problems. If the catheter is replaced, patient will continue on the same arm of the study. Control Group: We will lock the dialysis catheter post HD with TauroLock Hep500 at the end of of all Hemodialysis sessions and during all interdialytic periods. Intervention Group: We will lock the dialysis catheter post HD with TauroLock Hep500 at the end of the first two session only per week and during first two interdialytic periods then TauroLock U 25000at the end of third session before week end, (over the week end). For episode of the acute catheter malfunctioning:- The study coordinator will know the name of the patients who received interdialytic r-TPA from medication room then will collect the data from the patient's files. The study coordinator will follow the vascular census on daily bases to know all the patients who have catheter problems and will follow their status from dialysis and inpatient files. For catheter related infection:- If there is any episode of CRI, this will be documented in our infectious control file and the study coordinator will collect the data from in-patient file, dialysis file and medicom. planned enrollment: 300 subjects

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemodialysis, Tunneled Catheter, Qatar

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
170 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Active Comparator
Arm Description
We will lock the dialysis catheter post HD with TauroLock Hep500 at the end of of all Hemodialysis sessions and during all interdialytic periods
Arm Title
B
Arm Type
Experimental
Arm Description
We will lock the dialysis catheter post HD with TauroLock Hep500 at the end of the first two session only per week and during first two interdialytic periods then TauroLock U 25000at the end of third session before week end, (over the week end).
Intervention Type
Drug
Intervention Name(s)
TauroLock U 25000
Intervention Description
taurolidine citrate, 4% citrate /25000 IU unit urokinase (TauroLock U25000
Intervention Type
Drug
Intervention Name(s)
(TauroLock Hep500)
Intervention Description
1.35% taurolidine citrate (2H-1,2,4-thiadiazine-4,4'-methylenebis[tetrahydro-1,1,1',1'-tetraoxide], 4% citrate and 500 IU/ml heparin (TauroLock Hep500) (TauroPharmGmbH
Primary Outcome Measure Information:
Title
Number of catheter thrombosis episodes
Description
The time to first episode of catheter thrombosis lead to catheter change. Number of acute episode of thrombosis that interrupt dialysis Median Survival life of the catheter in both groups after adjusting it to the outcome.
Time Frame
6 months per patient
Secondary Outcome Measure Information:
Title
Amount of r-TPA used in each group for treatment of acute catheter thrombosis
Description
as above
Time Frame
6 months
Title
Number of catheter exchange in each group
Time Frame
6 months
Title
Hospitalization days related to catheter malfunctioning or CRI in each group
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1- Adult patients aged>14 years 2- Undergoing HD through tunneled HD 3- Recently inserted or old tunneled catheter 4- Blood flow rate at the beginning of the study≥ 300ml/min Exclusion Criteria: 1- Malfunctioning catheter defined by blood flow rate < 300ml/min 2- Known patient to have allergy to drug medication 3- Major Hemorrhage in previous 4 week
Facility Information:
Facility Name
Fahd Bin Jassem Dialysis Centre
City
Doha
ZIP/Postal Code
30550
Country
Qatar

12. IPD Sharing Statement

Plan to Share IPD
Yes

Learn more about this trial

Management of Tunneled Catheter Thrombosis in Hemodialysis Patients: Prospective Study From Qatar

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