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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02981732
Other study ID # 81674007
Secondary ID
Status Recruiting
Phase N/A
First received November 23, 2016
Last updated March 24, 2017
Start date October 2016
Est. completion date December 2020

Study information

Verified date March 2017
Source Fujian Academy of Traditional Chinese Medicine
Contact Yao xin
Phone 0591-83570813
Email yjyllbgs@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

For nearly 112 million patients with osteoporosis in China, it is of great significance for preventing and treating by clearly understanding the molecular mechanism of kidney deficiency. Thus, the research group has demonstrated in the earlier research that CLCF1 is an associated gene that can regulate JAK2/STAT3 signal pathway and impact bone metabolism for kidney yin deficiency of postmenopausal osteoporosis (PMOP). To make clear understanding of the direct-acting mechanism of CLCF1 for bone metabolism, this study intends to: ①observe impacts of low expression of CLCF1 upon immunities in mice and OPG/RANKL/RANK signal system using the technology of adenovirus associated virus. ②explore impacts of over-expression and silencing of CLCF1 on B lymphocytes by culcuturing the cells together with osteoblasts. ③ analyze the impacts of treating kidney yin deficiency of PMOP by Liuwei Dihuang pill upon immunities and OPG/RANKL/RANK system, and discuss the mechanism of regulating bone metabolism by CLCF1 by OPG/RANKL/RANK system via the bridge between immune system and bone metabolism, so as to demonstrate if the hypothesis of this study that "the molecular osteoimmunological mechanism of kidney yin deficiency of postmenopausal osteoporosis (PMOP) is possibly closely related to the impacts of CLCF1 regulation of OPG/RANKL/RANK signal system on bone metabolism" is right or not.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date December 2020
Est. primary completion date March 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 46 Years to 75 Years
Eligibility Inclusion Criteria:

- Patients were included if they were female Han Chinese patients who had undergone natural menopause at least 2 years prior and

- met the diagnostic criteria for osteoporosis according to the "clinical practice guidelines of traditional medicine for primary osteoporosis"

- met the CM diagnostic criteria according to "Syndrome Differentiation in Modern Research of Traditional Chinese Medicine"

- provided informed consent, which was approved by the Fujian Academy of Traditional Chinese Medicine Clinical Research Ethics Committee

Exclusion Criteria:

- patients who did not meet the diagnostic criteria for osteoporosis or CM standards

- patients with rheumatoid arthritis, diabetes, secondary osteoporosis due to hyperthyroidism, and severe cardiovascular or cerebrovascular diseases

- patients with abnormal liver and/or Shen function test results

- patients with osteoporosis who had received treatment with CM within the last month, hormone replacement therapy and calcitonin within the past three months, or bisphosphonates for 15 consecutive days within the past 6 months.

Study Design


Intervention

Other:
Liuwei Dihuang Pill


Locations

Country Name City State
China Fujian Academy of Trational Chiness Medicine Fuzhou Fujian

Sponsors (1)

Lead Sponsor Collaborator
xuhuijuan

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary osteoporosis treatment within six months of study enrollment Liuwei Dihuang Pills therapy(up to six months)
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