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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04145492
Other study ID # 12
Secondary ID
Status Recruiting
Phase Phase 2/Phase 3
First received
Last updated
Start date September 1, 2019
Est. completion date February 1, 2020

Study information

Verified date October 2019
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to assess the effect of supplementation of vitamin K2 (menaquinone, MK-7) and cholecalciferol (inactive vitamin D) on circulating levels of calcification regulators and to assess their safety in pediatric patients on regular hemodialysis patients.


Description:

Vascular calcification occurs in more than half of chronic renal failure patients, which mainly appears in the large and medium size arteries [3, 4]. It seems that vas¬cular calcification is caused by dynamic imbal-ance of intravascular calcium and phosphorus. However, more and more studies pointed out that vascular calcification were related with local cell's function and biological characteris¬tics.

The aim of this study is to assess the effect of supplementation of vitamin K2 (menaquinone, MK-7) and cholecalciferol (inactive vitamin D) on circulating levels of calcification regulators and to assess their safety in pediatric patients on regular hemodialysis patients.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date February 1, 2020
Est. primary completion date January 1, 2020
Accepts healthy volunteers No
Gender All
Age group 6 Years to 18 Years
Eligibility Inclusion criteria:

- Patients aged 6-18 years

- Patients on hemodialysis since 3 months or longer

- Hemodialysis frequency 3 times or more weekly

Exclusion criteria:

- Patients with life expectancy < 3 months

- Patients taking warfarin

- Patients with known intestinal malabsorption

Study Design


Intervention

Drug:
Vitamin K2
Patients will take 90 ug of vitamin K2
Cholecalciferol (inactive vitamin D)
Patients will take 10 ug of vitamin inactive vitamin D
Vitamin K2 and Cholecalciferol
Patients will take 90 ug of vitamin K2 (MK-7) in addition 10 ug of vitamin inactive vitamin D

Locations

Country Name City State
Egypt Radwa Maher El Borolossy Cairo

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Uncarboxylated MGP Measuring serum level of Uncarboxylated MGP as a marker for calcification 4 months
Primary Uncarboxylated osteocalcin Measuring serum level of Uncarboxylated osteocalcin as a marker for calcification 4 months
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