Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT05899283 |
Other study ID # |
S2021-171-01 |
Secondary ID |
|
Status |
Completed |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
March 1, 2021 |
Est. completion date |
October 30, 2022 |
Study information
Verified date |
June 2023 |
Source |
Chinese PLA General Hospital |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
This study exploring the expression characteristics of different cells of peripheral blood
after exposure to two kinds of hemodialysis filter membrane materials will help to elucidate
the key mechanisms of hemodialysis filter coagulation occurrence, which is an important
guideline for reducing the occurrence of adverse events in hemodialysis.
Description:
Background: Hemodialysis is one of the important alternative treatments for patients with
uremia, and effective hemodialysis treatment can improve mortality and quality of life.
However, during hemodialysis treatment, contact between blood and artificial materials often
triggers a coagulation cascade reaction, which induces dialyzer coagulation. Studies have
found that the incidence of dialyzer coagulation ranges from 5% to 14%. Once coagulation
occurs, it inevitably affects the efficiency of the patient's dialysis and may lead to
interruption of dialysis and blood loss, with the serious possibility of systemic
thromboembolic events. To prevent clotting, systemic anticoagulation is usually required,
which inevitably increases the risk of bleeding and lacks safe and effective anticoagulation
methods. Some studies have suggested that the endogenous coagulation pathway is the primary
pathway of dialyzer coagulation and that coagulation is effectively prevented by the use of
antibodies to coagulation factor F Ⅻ during extracorporeal circulation. Some studies,
however, suggest that the exogenous coagulation pathway is the primary pathway of dialyzer
coagulation. An in-depth study of coagulation activation will help us to understand the true
mechanism of dialyzer coagulation occurrence and provide new targets for the prevention and
treatment of coagulation during dialysis.
Methods: The study population consisted of 10 patients with uremia newly placed on
hemodialysis treatment for the first time. Inclusion criteria: 1.70 years ≥age ≥ 18 years,
gender not limited; 2.Patients with clinical diagnosis of chronic renal insufficiency (CKD
stage 5) requiring renal replacement therapy; 3.Dialysis access was central venous catheter;
4.Newly placed tubing, not dialysed patients; 5.Patients voluntarily participated and written
informed consent signed by the patient or authorized delegate had been obtained.Exclusion
criteria: 1.Patients with acute renal failure; 2.Patients are participating in other clinical
studies; 3.Pregnancy or breastfeeding; 4.Use of hemostatic or anticoagulant drugs in the last
1 week; 5.Positive infectious serum markers for HIV, syphilis, hepatitis B, and hepatitis C;
6. Presence of active infection; 7.Allergy to dialyzers.Observation index: Peripheral blood
before and after dialysis and filter after dialysis were collected, and blood routine,
coagulation factors, single cell sequencing and electron microscopy were performed to compare
the changes of coagulation factor activity before and after contact with dialysis membrane,
and to screen the major coagulation factors and coagulation pathway activation pathways.
Single-cell transcriptome characteristics of peripheral blood mononuclear cells before and
after exposure to dialysis membranes were analyzed to explore the key mechanisms of
peripheral blood cells regulating coagulation contact activation. Statistical methods: SPSS
version 17.0 statistical software was applied for statistical analysis, and continuous
variables were expressed as mean ± standard deviation, and non-continuous variables were
expressed as percentages. Comparisons between two data were made by independent t-test or χ2
test, and P<0.05 was statistically significant.