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Analysis of Protein Expression in Serum of KOA Subjects

C

China Medical University

Status

Enrolling

Conditions

Knee Osteoarthritis

Treatments

Device: Micro-Western Array

Study type

Interventional

Funder types

Other

Identifiers

NCT06553313
CMUH113-REC3-115

Details and patient eligibility

About

In the previous study "Using omics technology to explore the mechanism of acupuncture treatment of different acupoints of knee osteoarthritis: a randomized controlled trial (CMUH109-REC3-113)", we found that acupuncture for knee osteoarthritis(KOA) significantly reduces inflammation, apoptosis, and metabolism-related serum protein profiles. However, due to the lack of serum protein data from the control group, it is impossible to establish standard values for comparison. To analyze the protein expression in the serum of KOA control group subjects, we also measured the spectral energy values of the radial artery pulse wave obtained from the pulse sphygmograph and the meridian energy values obtained from Ryodoraku. The results obtained can be compared with previous studies, thus this experiment was designed.

Enrollment

50 estimated patients

Sex

All

Ages

50+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adults over 50 years old without knee pain

Exclusion criteria

  1. Clinical diagnosis of knee osteoarthritis
  2. Taking anti-inflammatory and analgesic drugs in the past month
  3. Taking blood-lipid-lowering drugs or health foods in the past month
  4. Received any acupuncture treatment in the past 3 weeks

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

50 participants in 1 patient group

the control group of knee arthritis
Other group
Description:
Monitoring the stability of protein expression, pulse wave and meridian energy in the serum of the KOA control group (participants without knee pain).
Treatment:
Device: Micro-Western Array

Trial contacts and locations

1

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Central trial contact

Wan-Zhen Yu; Yu-Chen Lee

Data sourced from clinicaltrials.gov

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