Effect of Astaxanthin in Moderate to Severe Knee Osteoarthritis
NCT ID: NCT05437601
Last Updated: 2024-04-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
80 participants
INTERVENTIONAL
2022-07-31
2022-12-19
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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Astaxanthin
Patients will receive three capsules of astaxanthin (4mg) daily for 8 weeks.
Astaxanthin Oral Capsule
12 mg oral astaxanthin daily for 8 weeks
Control
Patients will receive three capsules of placebo daily for 8 weeks.
Placebo
Oral placebo identical to astaxanthin
Interventions
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Astaxanthin Oral Capsule
12 mg oral astaxanthin daily for 8 weeks
Placebo
Oral placebo identical to astaxanthin
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Radiographic evidence of moderate to severe knee osteoarthritis
* Age 40 years or older
* Both male and female
Exclusion Criteria
* Previously diagnosed of systemic inflammatory conditions such as rheumatoid arthritis, systemic lupus erythematosus, inflammatory bowel disease
* Known allergy to fish or astaxanthin
* Currently taking immunosuppressant
* Pregnant and nursing mother
* Patients unwilling to participate or unwilling to give written consent
40 Years
90 Years
ALL
No
Sponsors
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Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh
OTHER
Responsible Party
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Masuma Tabassum
Investigator
Principal Investigators
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Masuma Tabassum, MBBS
Role: PRINCIPAL_INVESTIGATOR
Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh
Locations
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Bangabandhu Sheikh Mujib Medical University
Dhaka, , Bangladesh
Countries
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Other Identifiers
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BSMMU/2022/5680
Identifier Type: -
Identifier Source: org_study_id
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