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Completed

NCT Number: NCT04110847

Traditional Chinese Medicine Formula in the Treatment of Osteoarthritis of Knees or Hips.

To investigate the efficacy and safety of OA1 Extract capsules in the treatment of patients with knee or hip osteoarthritis (OA).

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Key information

Age range

20 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

About this study

This trial was a 12 weeks' randomized, double-blind, placebo-controlled study. The study was approved by the Institutional Review Board of Chung Shan Medical University hospital, and signed informed consent was obtained from each patient. Sixty patients of osteoarthritis of knees or hips were enrolled in this study. Inclusion criteria were: age 20 to 80 years; primary osteoarthritis in at least 1 knee or hip, verified; at least moderate pain during 2 weeks before random assignment to treatment, as identified by the Western Ontario and McMaster Universities (WOMAC) LK3.0 Osteoarthritis Index pain subscale for more than 4.

Primary outcome measures were WOMAC at week 12.

Secondary outcome measures were WOMAC at week 4 and 8; Visual analogue scale (VAS) , Quality of life by SF-36, patient global assessment (PGA), at week 4, 8 and 12; serum levels of osteocalcin, C-terminal telopeptide(CTX), Hs-CRP, and ESR.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 1. Age ≥20 years old 2. Written informed consent obtained 3. Been diagnosed with knee or hip osteoarthritis 4. The physician interpretation of X-ray identification and joint space narrowing or bone spurs confirmed 5. In randomized trials before entering if used steroids or non-steroid medications osteoarthritis stable doses required at least one week 6. The WOMAC osteoarthritis index of the degree of pain assessment in the past two weeks at least> 4ppm pain

Exclusion criteria

  • 1. Pregnant or breast-feeding women. 2. Chemotherapy or radiation therapy in cancer patients

Treatment and study plan

JING CEIH SHERN YUAN EXTRACT PILL

Drug

Oral use, 3#BID

Primary outcomes

  1. Western Ontario and McMaster Universities (WOMAC)

    Time frame: week 0, week 12

    The investigators use WOMAC to compared the difference between the week 12 and week 0

Secondary outcomes

  1. serum osteocalcin level

    Time frame: week 0, week 12

    The investigators use serum osteocalcin level to compared the difference between week 12 and week 0

  2. serum C-terminal telopeptide (CTX) level

    Time frame: week 0, week 12

    The investigators use serum CTX level to compared the difference between week 12 and week 0

  3. Western Ontario and McMaster Universities (WOMAC)

    Time frame: week 0, week 4, week 8

    The investigators use WOMAC to compared the difference between the week 4 and week 0, week 8 and week 0

  4. Visual Analog Scale for pain (VAS)

    Time frame: week 0, week 4, week 8, week 12

    The investigators use VAS to compared the difference between the week 4 and week 0, week 8 and week 0, week 12 and week 0

  5. Physicians Global Assessment to measure quality of life (PGA)

    Time frame: week 0, week 4, week 8, week 12

    The investigators use PGA to compared the difference between the week 4 and week 0, week 8 and week 0, week 12 and week 0

  6. Quality of life by SF-36

    Time frame: week 0, week 4, week 8, week 12

    The investigators use SF-36 to compared the difference between the week 4 and week 0, week 8 and week 0, week 12 and week 0

  7. High sensitivity C-reactive protein (Hs-CRP)

    Time frame: week 0, week 12

    The investigators use Hs-CRP to compared the difference between the week 12 and week 0

  8. Erythrocyte sedimentation rate (ESR)

    Time frame: week 0, week 12

    The investigators use ESR to compared the difference between the week 12 and week 0

Sponsors and collaborators

Lead sponsor

Chung Shan Medical University

Other

Registry information

Official study title

Traditional Chinese Medicine Formula in the Treatment of Osteoarthritis of Knees or Hips. A Randomized Double-Blind, Placebo-Controlled Clinical Trial.

Important dates

Study start
2010
Primary completion
2011
Study completion
2012
First posted
Oct 1, 2019
Registry last updated
Oct 1, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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