Effect of deer bone powder supplementation in knee osteoarthritis

Effect of deer bone powder supplementation in knee osteoarthritis: a randomized, double-blind, controlled study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0001030

Enrollment

Registered

2014-03-18

Start date

2014-01-27

Completion date

Unknown

Last updated

2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Dietary Supplement : Consumption of deer bone powder supplementation or placebo for 12 weeks (twice a day)

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Voluntarily agree to participate and sign in informed consent form 2) Adults aged over 50 3) Subject with discomfort at joint

Exclusion criteria

Exclusion criteria: 1) Subject with Kellgren-Lawrence grade 3 or 4 2) Comsumption of NSAID drugs within 1 weeks before the first visit 3) Suspected cases of inflammatory arthritis (raised ESR or CRP) 4) Those with a BMI over 30kg/m^2 5) Abnormality in nervous system or lower limb joint that can develope gait disturbance 6) Moderate to severe low back pain with or without radicular pain 7) Severe neurological and vascular disease 8) History of relevant test food allergies 9) Subjects who have experience to participate in other clinical trial within 4 weeks prior to study 10) Subjects whom the investigators judge as inproper to participate in this clinical trial

Design outcomes

Primary

Measure	Time frame
Questionnaire for joint health	—

Secondary

Measure	Time frame
Biomarker in blood and urine	—

Countries

Korea, Republic of

Contacts

Public ContactNahee Ryu

Ewha Womans University

Outcome results