To Investigate the Efficacy and Mechanism of ZBP Powder Product in the Treatment of Osteopenia in Patients With Pain.
Primary Purpose
Osteopenia
Status
Unknown status
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Placebos
Zhibai Dihuang powder
Sponsored by
About this trial
This is an interventional treatment trial for Osteopenia
Eligibility Criteria
Inclusion Criteria:
- aged 50 years or older.
- VAS score≧4.0 in a week.
- bone mineral density (BMD) of all participants was -2.5 or below.
Exclusion Criteria:
- diabetes.
- thyroidism function disorder.
- parathyroidism function disorder.
- liver or kidney function disorder.
- ovariectomy
- rheumatoid arthritis.
- bone cancer.
- ever used hormone agent within 6 months before assignment to treatment.
- ever used steroids more than 3 months before assignment to treatment.
- ever used analgesics, excepted acetaminophen, more than 1 week before assignment to treatment.
Sites / Locations
- WanFangHRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Zhibai Dihuang powder
placebos
Arm Description
Arm: Experimental: Zhibai Dihuang Formula powder Zhibai Dihuang Formula powder: Traditional Chinese medicine formula powder product 5g by mouth, after meal, 3 times in one day for 12 weeks
Arm: placebo Comparator placebos 5g by mouth after meal, 3 times in one day for 12 weeks
Outcomes
Primary Outcome Measures
Pain on the visual-analogue scales (VAS) for back and legs.
A VAS is a 100-mm-long horizontal line that is anchored by word descriptors at each end (no pain and worst pain possible). The patient selects the point on the line that best represents his or her perception of their pain level.
Secondary Outcome Measures
Full Information
NCT ID
NCT03245710
First Posted
February 24, 2017
Last Updated
April 27, 2020
Sponsor
Taipei Medical University WanFang Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03245710
Brief Title
To Investigate the Efficacy and Mechanism of ZBP Powder Product in the Treatment of Osteopenia in Patients With Pain.
Official Title
To Investigate the Efficacy and Mechanism of ZBP Powder Product in the Treatment of Osteopenia in Patients With Pain.
Study Type
Interventional
2. Study Status
Record Verification Date
April 2020
Overall Recruitment Status
Unknown status
Study Start Date
February 8, 2017 (Actual)
Primary Completion Date
May 7, 2020 (Anticipated)
Study Completion Date
March 7, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Taipei Medical University WanFang Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study investigates the efficacy and mechanism of traditional Chinese medicine formula power product in the treatment of osteopenia in patients with pain. Half of participants will receive Chinese medicine formula power product, while the other half will receive a placebo.
Detailed Description
Osteoporosis is a major public health problem, resulting in potentially pain and increasing risk of fracture. Treatment of osteoporosis consists of pharmacotherapy, lifestyle measures, dietary changes, mineral supplementation. Traditional Chinese medicine is a major component of health care in Taiwan and provides one treatment alternative for osteoporosis.
Investigators investigate the efficacy and mechanism of traditional Chinese medicine formula powder product in the treatment of osteopenia patients with pain.This trial is a 12 weeks' randomized, placebo-controlled study. The study was approved by the Wan Fang hospital, and signed informed consent was obtained from each participant. 80 Osteopenia participants with pain were enrolled in this study. There were 80 participants aged 50 years or older included. Before random assignment to treatment, participants were at least moderate pain during 2 weeks as identified by visual analogue scale (VAS) for more than 4. Bone mineral density (BMD) of all participants was -2.5 or below without diabetes, hyperthyroidism, hypoparathyroidism, liver or kidney function disorder, ovariectomy, rheumatoid arthritis, bone cancer, ever used hormone agent within 6 months before assignment to treatment, ever used steroids more than 3 week before assignment to treatment, Primary outcome measures were the change of VAS scale, Oswestry Disability Index and WHOQOL-BREF Taiwan at week 1 and 12. Secondary outcome was the genetic loci associated with a susceptibility to osteoprosis treated by traditional Chinese medicine formula powder product.
Result : To provide evidence of the efficacy and mechanisms of ZBP powder product in the treatment of osteoporosis patients with pain.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteopenia
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
80 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Zhibai Dihuang powder
Arm Type
Experimental
Arm Description
Arm: Experimental: Zhibai Dihuang Formula powder Zhibai Dihuang Formula powder: Traditional Chinese medicine formula powder product 5g by mouth, after meal, 3 times in one day for 12 weeks
Arm Title
placebos
Arm Type
Placebo Comparator
Arm Description
Arm: placebo Comparator placebos 5g by mouth after meal, 3 times in one day for 12 weeks
Intervention Type
Other
Intervention Name(s)
Placebos
Intervention Description
starch
Intervention Type
Dietary Supplement
Intervention Name(s)
Zhibai Dihuang powder
Intervention Description
the Traditional Chinese Medicine Formula Powder Product
Primary Outcome Measure Information:
Title
Pain on the visual-analogue scales (VAS) for back and legs.
Description
A VAS is a 100-mm-long horizontal line that is anchored by word descriptors at each end (no pain and worst pain possible). The patient selects the point on the line that best represents his or her perception of their pain level.
Time Frame
baseline and week 12
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
aged 50 years or older.
VAS score≧4.0 in a week.
bone mineral density (BMD) of all participants was -2.5 or below.
Exclusion Criteria:
diabetes.
thyroidism function disorder.
parathyroidism function disorder.
liver or kidney function disorder.
ovariectomy
rheumatoid arthritis.
bone cancer.
ever used hormone agent within 6 months before assignment to treatment.
ever used steroids more than 3 months before assignment to treatment.
ever used analgesics, excepted acetaminophen, more than 1 week before assignment to treatment.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Chung-Yu Huang, MD
Phone
+886-29307930
Ext
1710
Email
hcy@tmu.edu.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chung-Yu Huang, MD
Organizational Affiliation
Taipei Municipal WanFang Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
WanFangH
City
Taipei
ZIP/Postal Code
116
Country
Taiwan
Individual Site Status
Recruiting
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
To Investigate the Efficacy and Mechanism of ZBP Powder Product in the Treatment of Osteopenia in Patients With Pain.
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