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Neutrophil Gelatinase-associated Lipocalin VS Vascular Calcification in Maintenance Hemodialysis Patients (NGAL)

Primary Purpose

Chronic Kidney Disease-Mineral and Bone Disorder

Status
Not yet recruiting
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
palicalcitol
Sponsored by
Xiaoyan Jia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Chronic Kidney Disease-Mineral and Bone Disorder focused on measuring Chronic Kidney Disease-Mineral and Bone Disorder, Calcitriol Receptor, Lipocalin-2, Vascular Calcification

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria: Chronic kidney disease (CKD) maintenance hemodialysis patients with secondary hyperparathyroidism (SHPT), iPTH>300pg/ml Age 18-65 years old Haven't used anti-PTH agents within 3 months Signed informed consent Exclusion criteria: Allergic to vitamin D or similar drugs Vitamin D poisoning Expected survival is less than one year Acute inflammations, active liver disease, tumor, hospitalization within 3 months Fractures, major trauma or operations within 3 months.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Palicalcitol

    Arm Description

    Maintenance hemodialysis patients with secondary hyperparathyroidism (SHPT) treat with palicalcitol

    Outcomes

    Primary Outcome Measures

    Change from Baseline plasma NGAL levels at 12months
    Elisa

    Secondary Outcome Measures

    Change from baseline vascular calcification at 12months
    Coronary calcification scores (CACS) from serial computed tomographic images with the Agatston method is used to evaluate cardio-vascular calcification, 1 point=130~199HU;2 points=200~299HU;3 points =300~399HU;4 points≥400HU. Abdominal aortic calcification score (AACS) is measured by Kauppila method from lateral dual-energy X-ray absorptiometry spine, 0-3 points. Anterior chest radiographs is used to perform simple calcification scores for aortic arch knob, 0-100%. Higher scores mean a worse outcome.

    Full Information

    First Posted
    November 10, 2022
    Last Updated
    February 7, 2023
    Sponsor
    Xiaoyan Jia
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05720273
    Brief Title
    Neutrophil Gelatinase-associated Lipocalin VS Vascular Calcification in Maintenance Hemodialysis Patients
    Acronym
    NGAL
    Official Title
    The Effect of Neutrophil Gelatinase-associated Lipocalin Derived From Osteoblasts and Vascular Smooth Muscle Cells on Vascular Calcification in Chronic Kidney Desease and the Intervention of Paliscalcitol - Clinical Research Section
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    April 1, 2023 (Anticipated)
    Primary Completion Date
    March 31, 2024 (Anticipated)
    Study Completion Date
    March 31, 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor-Investigator
    Name of the Sponsor
    Xiaoyan Jia

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No

    5. Study Description

    Brief Summary
    The goal of this observational study or clinical trial is to learn about the effect of neutrophil gelatinase-associated lipocalin (NGAL) on vascular calcification in maintenance hemodialysis patients with secondary hyperparathyroidism (SHPT). The main question it aims to answer is: the predictive effects of blood NGAL level on the efficacy of palicalcitol in the treatment of SHPT and the adverse reactions of vascular calcification progression. Participants will be treated with palicalcitol, followed up and undergo routine series of Chronic Kidney Disease-Mineral and Bone Disorder associated tests before and after treatment.
    Detailed Description
    Sample size calculation: Because there was no previous study on the change of blood NGAL level in MHD patients with palicalcitol; refer to the NGAL changes before and after parathyroidectomy :N=12 NGAL715.84(578.73, 988.14)ng/mL before and 688.42(660.00, 760.26)ng/mL 4-7 days after surgery (p=0.071, paired T-test). According to the 20% loss rate; The sample size is finally determined to be 80 cases. Patients: maintenance hemodialysis patients with secondary hyperparathyroidism (SHPT). Palicalcitol injection Follow-up The patients are followed up for 1 year. Statistical methods All statistical tests are conducted by two-sided test, and the first type of error is 0.05 (α value) to determine the statistical significance of the difference. Quantitative data includ efficacy, laboratory test indicators, such as the number of cases, mean, median, standard deviation and range description. Qualitative data includ comorbidities, described in terms of frequency, composition or percentage. Statistical test: The parameter test method is preferred. If the data distribution differs greatly from the requirements of testing the hypothesis, the non-parameter test method will be used. Patients will be divided into two groups according to circulating NGAL levels before treatment; the clinical characteristics, changes of NGAL level, the efficacy of palicalcitol (changes of iPTH) and the main adverse reactions (increased blood calcium and phosphorus, progress of vascular calcification) are compared between two groups. T test or rank sum test are used for difference test. The correlation between blood NGAL level, VC score and CKD-MBD assay indexes is analyzed by pair-wise correlation and logistic multivariate regression.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Chronic Kidney Disease-Mineral and Bone Disorder
    Keywords
    Chronic Kidney Disease-Mineral and Bone Disorder, Calcitriol Receptor, Lipocalin-2, Vascular Calcification

    7. Study Design

    Primary Purpose
    Other
    Study Phase
    Phase 4
    Interventional Study Model
    Single Group Assignment
    Model Description
    Maintenance hemodialysis patients with secondary hyperparathyroidism
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    80 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Palicalcitol
    Arm Type
    Experimental
    Arm Description
    Maintenance hemodialysis patients with secondary hyperparathyroidism (SHPT) treat with palicalcitol
    Intervention Type
    Drug
    Intervention Name(s)
    palicalcitol
    Other Intervention Name(s)
    Calcitriol, Calcimimetics
    Intervention Description
    This study does not interfere with the clinical medication of the researchers, and the usage and dosage of the drugs will be recorded according to the actual use. The recommended starting dose of palicalcitol may be based on body weight, baseline iPTH, or combined with prior medication. Dose adjustment should be determined according to pre-dialysis iPTH, Ca and P. iPTH levels should be maintained at 150-300pg/ml, while Ca and P levels should be closely monitored. If hypercalcemia occurs, the dose should be reduced or medication should be discontinued until these parameters return to normal; Subsequently, the dose of palicalcitol should be restarted at a lower dose. If PTH levels decrease as a result of treatment, the dose of medication may need to be reduced accordingly. The dose adjustment interval is 2-4 weeks, and the dose can be adjusted immediately for safety reasons.
    Primary Outcome Measure Information:
    Title
    Change from Baseline plasma NGAL levels at 12months
    Description
    Elisa
    Time Frame
    12months
    Secondary Outcome Measure Information:
    Title
    Change from baseline vascular calcification at 12months
    Description
    Coronary calcification scores (CACS) from serial computed tomographic images with the Agatston method is used to evaluate cardio-vascular calcification, 1 point=130~199HU;2 points=200~299HU;3 points =300~399HU;4 points≥400HU. Abdominal aortic calcification score (AACS) is measured by Kauppila method from lateral dual-energy X-ray absorptiometry spine, 0-3 points. Anterior chest radiographs is used to perform simple calcification scores for aortic arch knob, 0-100%. Higher scores mean a worse outcome.
    Time Frame
    12months
    Other Pre-specified Outcome Measures:
    Title
    Change from baseline Chronic Kidney Disease-Mineral and Bone Disorder associated laboratory tests at 12months
    Description
    Serum calcium and phosphorus are analyzed by Beckman automatic biochemical analyzer in our laboratory center. Blood iPTH measured by ELISA.
    Time Frame
    12months
    Title
    Change from baseline bone density tests at 12months
    Description
    Quantitative computed tomography (QCT) measurements are performed at the lumbar spine (mean of L 1 and L 2 entire vertebral bodies, excluding posterior processes) and hip.
    Time Frame
    12months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion criteria: Chronic kidney disease (CKD) maintenance hemodialysis patients with secondary hyperparathyroidism (SHPT), iPTH>300pg/ml Age 18-65 years old Haven't used anti-PTH agents within 3 months Signed informed consent Exclusion criteria: Allergic to vitamin D or similar drugs Vitamin D poisoning Expected survival is less than one year Acute inflammations, active liver disease, tumor, hospitalization within 3 months Fractures, major trauma or operations within 3 months.

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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