Study of Tumor-shrinking Decoction (TSD) to Treat Symptomatic Uterine Fibroids
Primary Purpose
Leiomyoma
Status
Completed
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
TSD
Sponsored by
About this trial
This is an interventional treatment trial for Leiomyoma focused on measuring Leiomyoma, Medicine, Chinese Traditional, Randomized Controlled Trial
Eligibility Criteria
Inclusion Criteria:
- Premenopausal women aged 18 to 52 years; and
- have a primary diagnosis of symptomatic UFs based on clinical symptoms; and
- MRI examination as defined in the International Classification of Diseases (10th edition).
Exclusion Criteria:
- Unstable medical conditions such as serious cardiovascular diseases;
- With severe neuropsychiatric disorders;
- Combined with adenomyosis or other tumors;
- On treatment with Chinese medicine or other natural products in the previous 3 months;
- With an allergic history of herbal medicine; or
- Being pregnant and lactating women and those who currently use contraception.
Sites / Locations
- School of Chinese Medicine, University of Hong Kong
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
High dose TSD
Low dose TSD
Arm Description
Subjects in this arm receive high dose (217 g/day) TSD for 16 weeks.
Subjects in this arm receive low dose (69 g/day) TSD for 16 weeks.
Outcomes
Primary Outcome Measures
Changes in the symptom severity score of Uterine Fibroid Symptom and Quality of Life questionnaire (UFS-QOL) from Baseline to 6 months
UFS-QOL consists of 37 items to assess the severity of UFs-related symptoms and the quality of life of patients.
Secondary Outcome Measures
Change of clinical response from baseline on the the health-related quality of life of transformed UFS-QOL score
The secondary clinical outcome is the clinical response that is defined as a ≥30% baseline-to-endpoint reduction on the symptom severity of transformed UFS-QOL score.
Imaging outcomes
Imaging outcomes will be examined at baseline and endpoint using magnetic resonance imaging (MRI) scan to determine the number, size and density of the uterine fibroids.
Serum concentrations of estrogen and follicle-stimulating hormone
two blood samples will be collected from each patient at baseline and at the end of the study, respectively. The collection of blood will be conducted between 08:00 and 09:00 before meal. Sera will be separated and stored at -20ºC until assayed. Serum concentrations of estrogen, progesterone and follicle-stimulating hormone will be measured using chemiluminescent immunoassay (CLIA).
Full Information
NCT ID
NCT02189083
First Posted
May 14, 2014
Last Updated
October 27, 2020
Sponsor
The University of Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT02189083
Brief Title
Study of Tumor-shrinking Decoction (TSD) to Treat Symptomatic Uterine Fibroids
Official Title
A Double-blind, Randomized, Two-dose Trial of Tumor-shrinking Decoction (TSD), a Chinese Medicine Preparation in Patients With Symptomatic Uterine Fibroids
Study Type
Interventional
2. Study Status
Record Verification Date
July 2014
Overall Recruitment Status
Completed
Study Start Date
May 2014 (undefined)
Primary Completion Date
November 2015 (Actual)
Study Completion Date
February 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The University of Hong Kong
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
On the basis of empirical evidence and clinical practice, the investigators have developed a formula called Tumor-shrinking Decoction (TSD) used in the treatment of uterine fibroids (UFs). The investigators preliminary clinical observation has demonstrated the benefits of TSD in improving UFs.
TSD is composed of 15 individual Chinese medicines: Astragalus Membranaceus, Semen Coicis, Poria, Curcuma longa L, and Fritillaria Thunbergii Miq, Cassia twig, Pollen typhae, Resina draconis, Lithospermum erythrorhizon, Halloysitum Rubrum, Rhizoma Corydalis processed with vinegar, Hirudo, Calcined corrugated sub , Oyster Shell and Laminaria Japonica Aresch.
It is hypothesized that TSD can effectively reduce the fibroid size and improve the symptoms associated with UFs and the greater anti-tumor potency of TSD is associated with higher therapeutic doses.
To test this hypothesis, one 16-week, double-blind, randomized, two-dose trial will be conducted in patients with symptomatic UFs to determine whether the high dose (217 g/day) of TSD could produce significantly greater effects in reducing the fibroid size and improving its related symptoms and biochemical profiles compared to the lower dose (69 g/day).
Detailed Description
Numerous Chinese medicine preparations have been shown to possess therapeutic potential in relieving uterine fibroids (UFs) symptoms and shrinking the volume of fibroids without significant adverse effects, although the clinical efficacy needs to be further confirmed with rigorously designed.On the basis of empirical evidence and clinical practice, the investigators have developed a formula called Tumor-shrinking Decoction (TSD) used in the treatment of UFs. The investigators preliminary clinical observation has demonstrated the benefits of TSD in improving UFs.
TSD is composed of 15 individual Chinese medicines. According to traditional Chinese medicine (TCM) doctrine, most UFs are developed due to the deficiency of vital energy and the stasis of blood, resulting in the formation of pathological massive tissues. Individual Chinese medicines constituting TSD can be classified into three classes based on TCM-defined pharmacological actions: (i) Tonifying qi and resolve phlegm: Astragalus Membranaceus, Semen Coicis, Poria, Curcuma longa L, and Fritillaria Thunbergii Miq; (ii) Resolve stasis, stopping bleeding and relieve pain: Cassia twig, Pollen typhae, Resina draconis, Lithospermum erythrorhizon, Halloysitum Rubrum, Rhizoma Corydalis processed with vinegar; and (iii) Softening hardness and dissipate binds: Hirudo, Calcined corrugated sub , Oyster Shell and Laminaria Japonica Aresch.
Indeed, the investigators previous studies of cultured cells and animals have revealed that TSD robustly inhibits fibroid cell growth and proliferation. The investigators therefore hypothesize that TSD can effectively reduce the fibroid size and improve the symptoms associated with UFs and the greater anti-tumor potency of TSD is associated with higher therapeutic doses.
To test this hypothesis, one 16-week, double-blind, randomized, two-dose trial will be conducted in patients with symptomatic UFs to determine whether the high dose (217 g/day) of TSD could produce significantly greater effects in reducing the fibroid size and improving its related symptoms and biochemical profiles compared to the lower dose (69 g/day).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Leiomyoma
Keywords
Leiomyoma, Medicine, Chinese Traditional, Randomized Controlled Trial
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
78 (Actual)
8. Arms, Groups, and Interventions
Arm Title
High dose TSD
Arm Type
Experimental
Arm Description
Subjects in this arm receive high dose (217 g/day) TSD for 16 weeks.
Arm Title
Low dose TSD
Arm Type
Active Comparator
Arm Description
Subjects in this arm receive low dose (69 g/day) TSD for 16 weeks.
Intervention Type
Drug
Intervention Name(s)
TSD
Other Intervention Name(s)
Tumor-shrinking Decoction, Chinese medicine preparation
Intervention Description
TSD is composed of 15 individual Chinese medicines: Astragalus Membranaceus, Semen Coicis, Poria, Curcuma longa L, and Fritillaria Thunbergii Miq, Cassia twig, Pollen typhae, Resina draconis, Lithospermum erythrorhizon, Halloysitum Rubrum, Rhizoma Corydalis processed with vinegar, Hirudo, Calcined corrugated sub , Oyster Shell and Laminaria Japonica Aresch.
High dose (127g) or Low dose (69g) TSD decoction boiled as 200ml per bag; 2 bags per day, 6 days per week; Orally in-take one bag of TSD decoction in morning and another in evening after meal; The whole treatment lasts for 16 weeks.
Primary Outcome Measure Information:
Title
Changes in the symptom severity score of Uterine Fibroid Symptom and Quality of Life questionnaire (UFS-QOL) from Baseline to 6 months
Description
UFS-QOL consists of 37 items to assess the severity of UFs-related symptoms and the quality of life of patients.
Time Frame
Baseline and once per month thereafter; Up to 6 months
Secondary Outcome Measure Information:
Title
Change of clinical response from baseline on the the health-related quality of life of transformed UFS-QOL score
Description
The secondary clinical outcome is the clinical response that is defined as a ≥30% baseline-to-endpoint reduction on the symptom severity of transformed UFS-QOL score.
Time Frame
Baseline and once per month thereafter; Up to 6 months
Title
Imaging outcomes
Description
Imaging outcomes will be examined at baseline and endpoint using magnetic resonance imaging (MRI) scan to determine the number, size and density of the uterine fibroids.
Time Frame
Baseline, 5th month
Title
Serum concentrations of estrogen and follicle-stimulating hormone
Description
two blood samples will be collected from each patient at baseline and at the end of the study, respectively. The collection of blood will be conducted between 08:00 and 09:00 before meal. Sera will be separated and stored at -20ºC until assayed. Serum concentrations of estrogen, progesterone and follicle-stimulating hormone will be measured using chemiluminescent immunoassay (CLIA).
Time Frame
Baseline, 5th month
Other Pre-specified Outcome Measures:
Title
Number of Participants with Serious and Non-Serious Adverse Events
Description
Adverse events will be closely monitored at each visit. All adverse events, reported, elicited or observed, will be recorded on case report form, including the date and time of onset, duration, severity, relationship to study drug, and action taken.
Time Frame
Up to 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
52 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Premenopausal women aged 18 to 52 years; and
have a primary diagnosis of symptomatic UFs based on clinical symptoms; and
MRI examination as defined in the International Classification of Diseases (10th edition).
Exclusion Criteria:
Unstable medical conditions such as serious cardiovascular diseases;
With severe neuropsychiatric disorders;
Combined with adenomyosis or other tumors;
On treatment with Chinese medicine or other natural products in the previous 3 months;
With an allergic history of herbal medicine; or
Being pregnant and lactating women and those who currently use contraception.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wei Meng
Organizational Affiliation
The University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
School of Chinese Medicine, University of Hong Kong
City
Hong Kong
ZIP/Postal Code
852
Country
China
12. IPD Sharing Statement
Citations:
Citation
Lu J, Meng W. Clinical observation 45 cases of Yiqi Huayu treatment for uterine fibroids. Gansu TCM. 2008a;6:44-46
Results Reference
result
Citation
Lu J, Meng W. Clinical Observation of " Hualiu Recipe" in Treating 302 Cases of Hysteromyoma with Qi- Deficiency and Blood- Stasis Syndrome. Shanghai Traditional Chinese Medicine. 2008b;3:49-51
Results Reference
result
Citation
Meng W, Ma B. Three drugs on cultured uterine leiomyoma cell proliferation and apoptosis, and regulatory factors. Traditional Chinese. 2003;21:2046-2048
Results Reference
result
Citation
Meng W. Zhao W. Effects of methods of invigorating qi and dissolving stasis on the expression of proliferating and apoptosis of cultured human uterine leiomyoma cells. Chinese archives of traditional Chinese medicine. 2008(2);238-240
Results Reference
result
PubMed Identifier
21812264
Citation
Tan L, Meng W, Zhang TT. [Predisposing factors of hysteromyoma and effect of hualiu recipe on it]. Zhongguo Zhong Xi Yi Jie He Za Zhi. 2011 May;31(5):635-8. Chinese.
Results Reference
result
Links:
URL
http://www.asrm.org/FactSheetsandBooklets/
Description
American Society of Reproductive Medicine Patient Booklet: Uterine Fibroids
Learn more about this trial
Study of Tumor-shrinking Decoction (TSD) to Treat Symptomatic Uterine Fibroids
We'll reach out to this number within 24 hrs