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Role of Alphacalcidol Supplement to Reduce Pain and COMP in Geriatric Knee Osteoarthritis Patients

Primary Purpose

Osteoarthritis, Knee, Aged

Status
Completed
Phase
Phase 3
Locations
Indonesia
Study Type
Interventional
Intervention
Alfacalcidol 1 MCG Oral Capsule
Sugar pill
Sponsored by
Syarif Hidayatullah State Islamic University Jakarta
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis, Knee focused on measuring Vitamin D, Alfacalcidol, Knee osteoarthritis pain, Cartilage Oligomeric Matrix Protein

Eligibility Criteria

60 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with knee pain due to OA who meet clinical and radiological criteria according to Kellgren-Lawrence grade at least 1 month with knee pain of at least 5 measured using the WOMAC pain index
  • Body mass index ≤27 kg/m2
  • Do not have any systemic inflammatory diseases or other systemic diseases from history taking and physical examination
  • Do not have any other OA in other joints according to physical examination
  • Did not do any heavy physical activity or strenuous exercise for at least 1 month (last month)

Exclusion Criteria:

  • Grade 4 Kellgren-Lawrence
  • WOMAC pain score >15
  • Serum 25(OH)D >125 nmol/L
  • Calcium serum >10.5 mg/dl
  • Diagnosed with rheumatoid or psoriatic arthritis, lupus or cancer, heart or kidney disorders, vitamin D hypersensitivity.
  • Knee trauma, including injury to the ligament or meniscus before the study
  • Consuming drugs that contain Magnesium (Antacids), Digitalis (Digoxin), Barbiturates or other anti-convulsants for a long time, which will interact with Vitamin D
  • Currently undergoing vitamin D therapy for the last 30 days
  • Use of other supplements intended to have an effect on cartilage such as glucosamine and chondroitin sulphate
  • Undergo intra-articular therapy 3 months before the study
  • Consume oral corticosteroids
  • Senile dementia or other signs and symptoms of memory loss

Sites / Locations

  • Public Health Service Clinic Reni Jaya

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Intervention group

Control Group

Arm Description

Individuals in intervention group were given oral Vitamin D supplements (Alphacalcidol 1 µg) once daily

Individuals in control group were given placebo once daily

Outcomes

Primary Outcome Measures

WOMAC Pain Score Difference
Instrument for assessing pain in knee OA patients from The Western Ontario & McMaster University OA Index. WOMAC pain score was assessed every 2 weeks to ensure that subject's pain within inclusion criteria.
Cartilage Oligomeric Matrix Protein Difference
Serum concentration of Cartilage Oligomeric Matrix Protein (COMP) as a biomarker for the severity of knee OA.

Secondary Outcome Measures

Serum 25(OH)D Concentration Difference
Serum 25(OH)D Concentration as vitamin D deficiency status
Body Mass Index
Body mass index, calculated by measuring subject's height and weight
Kellgren-Lawrence Knee OA Grade
Radiological knee OA grading system
Mean Physical Activity
Physical activities performed by subjects using their energy related to work and daily leisure time. Measured using Basic Health Research (Riskesdas) 2007 Questionnaire
Mean Sun Exposure Frequency
Ultraviolet B (UVB) exposure between 7-11 am for ≥ 30 minutes with exposure at least to the face and palms
Mean Vitamin D Consumption
The amount of Vitamin D consumption by subjects, which is calculated based on the consumption of fruits, vegetables, milk and its processed products, fish, etc.

Full Information

First Posted
May 14, 2020
Last Updated
May 22, 2020
Sponsor
Syarif Hidayatullah State Islamic University Jakarta
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1. Study Identification

Unique Protocol Identification Number
NCT04405960
Brief Title
Role of Alphacalcidol Supplement to Reduce Pain and COMP in Geriatric Knee Osteoarthritis Patients
Official Title
Role of Vitamin D (Alphacalcidol) Supplement to Reduce Pain and Cartilage Oligomeric Matrix Protein Serum Levels in Geriatric Knee Osteoarthritis Patients: A Randomized, Double-Blind, Placebo-Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Completed
Study Start Date
July 1, 2017 (Actual)
Primary Completion Date
September 30, 2017 (Actual)
Study Completion Date
December 31, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Syarif Hidayatullah State Islamic University Jakarta

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Indonesian population's life expectancy has been increasing steadily in the last 3 decades. It potentially increases the prevalence of degenerative diseases, including osteoarthritis (OA). Serum Vitamin D (25(OH)D) level has been recognized as a risk factors for knee OA. Cartilage Oligomeric Matrix Protein (COMP) is cartilage degradation product can be used as a diagnostic marker for knee OA. This study aims to determine the effect of Vitamin D supplementation (Alphacalcidol) on pain based on WOMAC indicators and joint cartilage condition based on COMP serum markers in knee OA elderly patients.
Detailed Description
Vitamin D plays important role to enhance calcium absorption in intestine and promotes mineralization of bones. Several studies found that Vitamin D levels were low in patients with knee OA. Vitamin D deficiency were found in 50% of women age 45-55 years old and 35% of women age 60-90 years old in Jakarta and Bekasi. Alphacalcidol is a vitamin D supplementation recommended to be used in patients with renal insufficiency, which is prevalent in elderly. Alfacalcidol does not need to undergo renal 1-alpha-hydroxylation which impaired in renal insufficiency, although it can still cause hypercalcemia. Current detection and diagnosis of knee OA relies on plain radiological examination, which is not really objective because it depends on radiological expertise and experience. Moreover, plain radiological diagnosis has limited ability to detect joint damage at an early stage. Therefore, knee OA is often diagnosed at advanced stage. For this reason, selecting accurate joint cartilage biomarkers is important to detect and predict the severity of OA objectively and at earlier stage. Cartilage Oligomeric Matrix Protein (COMP) is one of degradation products released into synovium fluid and bloodstream from cartilage matrix turnover process. Therefore, COMP can be used as a marker of diagnosis and cartilage injury severity of knee OA. Currently, there has been no study about the association of Vitamin D supplementation with pain level and cartilage matrix turnover process in Indonesia. Therefore, this study aims to determine the effect of Vitamin D supplementation (Alphacalcidol) on pain and joint cartilage condition in elderly patients with knee OA.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Knee, Aged
Keywords
Vitamin D, Alfacalcidol, Knee osteoarthritis pain, Cartilage Oligomeric Matrix Protein

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
This is a randomized, double-blind, and placebo-controlled trials. Elderly subjects with symptomatic knee OA visited our clinic in Jakarta were recruited. Medical history taking, physical examinations, knee radiology, blood test for Vitamin D (25(OH)D), calcium, and COMP serum were performed. Subjects were then randomly allocated to either intervention group to be given 1 µg Alphacalcidol or control group to be given placebo in 12 weeks.
Masking
ParticipantCare ProviderInvestigator
Masking Description
This study used Contract Research Organization (CRO) Equilab to ensure the quality. In this study, researchers, respondents, interviewers, supplement providers, radiology and laboratory staffs were blinded. The interviewers used a questionnaire that had been prepared previously and was used equally for the intervention and control groups. Knee x-ray examination was performed to determine knee OA severity based on Kellgren-Lawrence grading system. It was carried out using the same method and technique between the intervention and control groups. X-ray examination was carried out at the same hospital's radiology unit and was interpreted blindingly by the same radiologist. Blood examination to measure 25(OH)D and COMP was carried out using the same methods and techniques between the intervention and control groups by staffs from the same certified laboratory.
Allocation
Randomized
Enrollment
146 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention group
Arm Type
Experimental
Arm Description
Individuals in intervention group were given oral Vitamin D supplements (Alphacalcidol 1 µg) once daily
Arm Title
Control Group
Arm Type
Placebo Comparator
Arm Description
Individuals in control group were given placebo once daily
Intervention Type
Drug
Intervention Name(s)
Alfacalcidol 1 MCG Oral Capsule
Other Intervention Name(s)
Bon-One, One-Alpha
Intervention Description
The subjects in the intervention group were given 1 µg oral capsule alphacalcidol once daily Subjects in the control group were given placebo once daily with similar capsule shape and color to the capsule given to the intervention group. The process of alphacalcidol and placebo encapsulation were carried out by pharmacists in the pharmacy depot under the supervision of researchers and CRO Equilab. Alphacalcidol and placebo were put into plastic pots containing 30 capsules for every 4 weeks for each subject. The pot had an etiquette written explaining how to consume the drug (after breakfast between 7 - 10 a.m.). The drugs' packaging and code numbering were carried out by CRO Equilab to ensure a double-blind procedure. As a control, each subject was equipped with a monitoring card. Alphacalcidol and placebo were given for 12 weeks without interruption. Monitoring of compliance and side effects was performed by physicians every 2 weeks.
Intervention Type
Drug
Intervention Name(s)
Sugar pill
Other Intervention Name(s)
Placebo
Intervention Description
The subjects in the control group were given placebo containing simple sugar oral capsule once daily with similar capsule shape and color to the capsule given to the intervention group. The process of alphacalcidol and placebo encapsulation were carried out by pharmacists in the pharmacy depot under the supervision of researchers and CRO Equilab. Alphacalcidol and placebo were put into plastic pots containing 30 capsules for every 4 weeks for each subject. The pot had an etiquette written explaining how to consume the drug (after breakfast between 7 - 10 a.m.). The drugs' packaging and code numbering were carried out by CRO Equilab to ensure a double-blind procedure. As a control, each subject was equipped with a monitoring card. Alphacalcidol and placebo were given for 12 weeks without interruption. Monitoring of compliance and side effects was performed by physicians every 2 weeks.
Primary Outcome Measure Information:
Title
WOMAC Pain Score Difference
Description
Instrument for assessing pain in knee OA patients from The Western Ontario & McMaster University OA Index. WOMAC pain score was assessed every 2 weeks to ensure that subject's pain within inclusion criteria.
Time Frame
Initial and final week (week 0 and 12).
Title
Cartilage Oligomeric Matrix Protein Difference
Description
Serum concentration of Cartilage Oligomeric Matrix Protein (COMP) as a biomarker for the severity of knee OA.
Time Frame
Initial and final week (week 0 and 12).
Secondary Outcome Measure Information:
Title
Serum 25(OH)D Concentration Difference
Description
Serum 25(OH)D Concentration as vitamin D deficiency status
Time Frame
Initial and final week (week 0 and 12).
Title
Body Mass Index
Description
Body mass index, calculated by measuring subject's height and weight
Time Frame
Once, on week-0
Title
Kellgren-Lawrence Knee OA Grade
Description
Radiological knee OA grading system
Time Frame
Once, on week-0
Title
Mean Physical Activity
Description
Physical activities performed by subjects using their energy related to work and daily leisure time. Measured using Basic Health Research (Riskesdas) 2007 Questionnaire
Time Frame
Every 2 weeks (from week-0 until week-12)
Title
Mean Sun Exposure Frequency
Description
Ultraviolet B (UVB) exposure between 7-11 am for ≥ 30 minutes with exposure at least to the face and palms
Time Frame
Every 2 weeks (from week-0 until week-12)
Title
Mean Vitamin D Consumption
Description
The amount of Vitamin D consumption by subjects, which is calculated based on the consumption of fruits, vegetables, milk and its processed products, fish, etc.
Time Frame
Every 4 weeks (from week-0 until week-12)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with knee pain due to OA who meet clinical and radiological criteria according to Kellgren-Lawrence grade at least 1 month with knee pain of at least 5 measured using the WOMAC pain index Body mass index ≤27 kg/m2 Do not have any systemic inflammatory diseases or other systemic diseases from history taking and physical examination Do not have any other OA in other joints according to physical examination Did not do any heavy physical activity or strenuous exercise for at least 1 month (last month) Exclusion Criteria: Grade 4 Kellgren-Lawrence WOMAC pain score >15 Serum 25(OH)D >125 nmol/L Calcium serum >10.5 mg/dl Diagnosed with rheumatoid or psoriatic arthritis, lupus or cancer, heart or kidney disorders, vitamin D hypersensitivity. Knee trauma, including injury to the ligament or meniscus before the study Consuming drugs that contain Magnesium (Antacids), Digitalis (Digoxin), Barbiturates or other anti-convulsants for a long time, which will interact with Vitamin D Currently undergoing vitamin D therapy for the last 30 days Use of other supplements intended to have an effect on cartilage such as glucosamine and chondroitin sulphate Undergo intra-articular therapy 3 months before the study Consume oral corticosteroids Senile dementia or other signs and symptoms of memory loss
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Achmad Zaki, PhD
Organizational Affiliation
Faculty of Medicine Syarif Hidayatullah State Islamic University Jakarta
Official's Role
Principal Investigator
Facility Information:
Facility Name
Public Health Service Clinic Reni Jaya
City
South Tangerang
State/Province
Banten
ZIP/Postal Code
15417
Country
Indonesia

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Author's informed consent does not include IPD sharing agreement.
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Role of Alphacalcidol Supplement to Reduce Pain and COMP in Geriatric Knee Osteoarthritis Patients

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