Three Anticoagulation Strategies for Hemodialysis in Patients at Risk of Hemorrhage (TASHA)
Primary Purpose
Hemodialysis, Anticoagulation
Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
two stage regional citrate
one stage regional citrate
Sponsored by

About this trial
This is an interventional treatment trial for Hemodialysis
Eligibility Criteria
Inclusion Criteria:
- age>=18 years
- intermittent hemodialysis patients that carry on a 4 hours hemodialysis procedure, 2-3 times one week.
- the therapy mode is hemodialysis,with a dialysis fluid more than 500ml/min and blood flow volume more than 3.5-4ml/min.kg;
- at risk of hemorrhage,including active hemorrhage(within 3 days),post-operation(within 3 days) and pre-invasive operation(within 7 days).
Exclusion Criteria:
- at high risk of citrate accumulation( total bilirubin >60umol/L; lactic acid>3mmol/L,);
- use the drugs that impact the coagulation function within 7 days;
- serious hypocalcemia (serum calcium<1.9mmol/L).
Sites / Locations
- Guangdong General HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Placebo Comparator
Active Comparator
Experimental
Arm Label
saline flushes
one stage regional citrate
two stage regional citrate
Arm Description
saline flushes with 250 mL were carried out every 30 min.
one stage regional citrate:4% trisodium citrate was infused at the arterial bubble trap at a rate according to the blood flow( 1.2 x blood flow)ml/h.
two stage regional citrate:4% trisodium citrate was infused at the arterial bubble trap at a rate according to the blood flow(3/4 x 1.2 x blood flow)ml/h,and at the venous bubble trap at a rate according to the blood flow(1/4 x 1.2 x blood flow)ml/h.
Outcomes
Primary Outcome Measures
therapy interruption event
visible serious circuit clotting or persistent alarms such as venous pressure (> 200 mmHg) or TMP (> 300 mmHg)dialyzer
Secondary Outcome Measures
the clotting scores
the clotting scores in the venous expansion chamber, arterial expansion chamber and dialyzer
urea clearance
the measurement of Kt/V and URR
Full Information
NCT ID
NCT03419923
First Posted
January 11, 2018
Last Updated
December 11, 2018
Sponsor
Guangdong Provincial People's Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03419923
Brief Title
Three Anticoagulation Strategies for Hemodialysis in Patients at Risk of Hemorrhage
Acronym
TASHA
Official Title
Three Anticoagulation Strategies for Hemodialysis in Patients at Risk of Hemorrhage: a Multicenter Randomized Trial
Study Type
Interventional
2. Study Status
Record Verification Date
December 2017
Overall Recruitment Status
Unknown status
Study Start Date
September 10, 2017 (Actual)
Primary Completion Date
March 30, 2019 (Anticipated)
Study Completion Date
March 30, 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Guangdong Provincial People's Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim of our study is to assess three anticoagulation strategies for intermittent hemodialysis(IHD) in patients at risk of hemorrhage. A registry of consecutive hemodialysis patients with high risk of hemorrhage was conducted at the Guangdong General Hospital, the First Affiliated Hospital of Guangzhou University of Chinese Medicine, the Second Affiliated Hospital of Guangzhou Medicine University or Guangzhou Hospital of Chinese Medicine, between Sep 10, 2017 and June 30th,2018. In this multi-center prospective and randomized study, participants were randomly divided into three groups during IHD according to different anticoagulation, including with regular saline flushes, one stage regional citrate anticoagulation (RCA) and two-stage RCA.
Detailed Description
Briefly, there are two parts in this study. The first part of the study is to compare two-stage RCA with one stage RCA during IHD, and the second part is to compare two-stage RCA with regular saline flushes, with estimated total procedures, 78 and 48, respectively. The primary outcome was measured as therapy interruption based on visible serious circuit clotting or persistent alarms such as venous pressure (> 200 mmHg) or TMP(transmembrane pressures) (> 300 mmHg). The secondary outcomes included circuit survival time, the total clotting score of ECC(extracorporeal circuit ) and urea clearance (Kt/V and URR). The total clotting score was the sum of the clotting scores for the venous expansion chamber, arterial expansion chamber, and dialyzer.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemodialysis, Anticoagulation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
141 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
saline flushes
Arm Type
Placebo Comparator
Arm Description
saline flushes with 250 mL were carried out every 30 min.
Arm Title
one stage regional citrate
Arm Type
Active Comparator
Arm Description
one stage regional citrate:4% trisodium citrate was infused at the arterial bubble trap at a rate according to the blood flow( 1.2 x blood flow)ml/h.
Arm Title
two stage regional citrate
Arm Type
Experimental
Arm Description
two stage regional citrate:4% trisodium citrate was infused at the arterial bubble trap at a rate according to the blood flow(3/4 x 1.2 x blood flow)ml/h,and at the venous bubble trap at a rate according to the blood flow(1/4 x 1.2 x blood flow)ml/h.
Intervention Type
Drug
Intervention Name(s)
two stage regional citrate
Intervention Description
4% trisodium citrate was infused at the arterial bubble trap at a rate according to the blood flow(3/4 x 1.2 x blood flow)ml/h,and at the venous bubble trap at a rate according to the blood flow(1/4 x 1.2 x blood flow)ml/h.
Intervention Type
Drug
Intervention Name(s)
one stage regional citrate
Intervention Description
4% trisodium citrate was infused at the arterial bubble trap at a rate according to the blood flow( 1.2 x blood flow)ml/h.
Primary Outcome Measure Information:
Title
therapy interruption event
Description
visible serious circuit clotting or persistent alarms such as venous pressure (> 200 mmHg) or TMP (> 300 mmHg)dialyzer
Time Frame
through study completion, from start to four hours
Secondary Outcome Measure Information:
Title
the clotting scores
Description
the clotting scores in the venous expansion chamber, arterial expansion chamber and dialyzer
Time Frame
through study procedure,an average of four hours
Title
urea clearance
Description
the measurement of Kt/V and URR
Time Frame
through study procedure,an average of four hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
age>=18 years
intermittent hemodialysis patients that carry on a 4 hours hemodialysis procedure, 2-3 times one week.
the therapy mode is hemodialysis,with a dialysis fluid more than 500ml/min and blood flow volume more than 3.5-4ml/min.kg;
at risk of hemorrhage,including active hemorrhage(within 3 days),post-operation(within 3 days) and pre-invasive operation(within 7 days).
Exclusion Criteria:
at high risk of citrate accumulation( total bilirubin >60umol/L; lactic acid>3mmol/L,);
use the drugs that impact the coagulation function within 7 days;
serious hypocalcemia (serum calcium<1.9mmol/L).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xinling Liang, Ph.D.,M.D.
Phone
+8613808819770
Email
13808819770@139.com
First Name & Middle Initial & Last Name or Official Title & Degree
Ting Lin, Ph.D.,M.D.
Phone
+8615013186074
Email
linting131@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Liming Yao, M.D.
Organizational Affiliation
Guangdong Provincial People's Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Guangdong General Hospital
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510515
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ting Lin, Ph.D.,M.D.
Phone
+8615013186074
Email
linting131@163.com
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Three Anticoagulation Strategies for Hemodialysis in Patients at Risk of Hemorrhage
We'll reach out to this number within 24 hrs