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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00912106
Other study ID # 96024
Secondary ID NSC-96-
Status Completed
Phase N/A
First received June 2, 2009
Last updated June 2, 2009
Start date April 2008
Est. completion date June 2009

Study information

Verified date June 2009
Source Far Eastern Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Observational

Clinical Trial Summary

To analyze the relationship between composition of synovial fluid and its lubrication properties


Description:

Patients suffering from serious arthritis may receive the artificial joint replacement surgery. Comparing to the articulation of articular cartilage, the artificial joint undergo a boundary lubrication in which a thin layer of synovial fluid molecules is formed between the artificial joint materials. Therefore a larger wear rate is observed in the artificial joint system. Researchers have devoted themselves to modifying the artificial joint materials in order to reduce the wear phenomena. We first propose that modification the lubrication by adding effective lubricating molecules may help to reduce the wear of artificial joint. However, there still lacks fundamentally understanding of the artificial joint lubrication mechanism under synovial fluid. Hence, we plan to investigate the boundary lubrication mechanism of synovial molecules, such as albumin, globulin, hyaluronic acid, and lipid in the first year. We would like to obtain the adsorption behaviors of the single molecules as well as multiple molecules on the surfaces of artificial joint materials by experiments. Molecular dynamics simulation will also be performed to gain the knowledge of adsorption energy and possible conformation change of the molecules. In the second year, the tribological heat and mechanical effects on the synovial molecules will be studied. The analysis platform will be established to perform the composition and properties measurement of the synovial molecules. In the third year, we will further discuss the effect of the synovial molecules transformation on the surrounding cells and tissues. Their influences on the tribological and biochemical behaviors will be investigated.


Recruitment information / eligibility

Status Completed
Enrollment 55
Est. completion date June 2009
Est. primary completion date December 2008
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients who are going to receive HA injection of one or two knees

Exclusion Criteria:

- Patients whose quantity of synovial fluid is not enough to be drawn

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Intervention

Other:
Synovial fluid composition and lubrication analysis
Before HA injection, synovial fluid must be drawn to increase treatment effectiveness. The drawn synovial fluid was then analyzed in the lab. There was no influence for patients enrolled because the drawn synovial fluid would usually be discarded.

Locations

Country Name City State
Taiwan Far Eastern Memorial Hospital Pan-Ciao Taipei

Sponsors (2)

Lead Sponsor Collaborator
Far Eastern Memorial Hospital National Science Concil

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Synovial fluid HA and albumin concentration; synovial fluid lubrication 1 wk, 2 wk, 3 wk, 4 wk, 5 wk Yes
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