Compound Herbal Formula (TPE-1) for Leukopenia and Cancer-related Fatigue in Breast Cancer Patients With Radiotherapy
Recruitment status was Recruiting
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Purpose
Many breast cancer patients will taking Chinese herbal medicine during receiving radiotherapy. The investigators conducted the pilot study showing Compound Herbal Formula (TPE-1) have the effect of improving the fatigue and leukopenia during radiotherapy. So the investigators designed this double blind and controlled trial to evaluate whether TPE-1 have the effects for leukopenia and cancer-related fatigue in breast cancer patients with radiotherapy. From our initial observation for 2 years, TPE-1 is safety. The study is also designed to evaluate the safety when patients taking this formula.
| Condition | Intervention | Phase |
|---|---|---|
|
Breast Cancer Radiotherapy Chinese Herbal Medicine |
Drug: Chinese herbal medicine decoction |
Phase 2 Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver) Primary Purpose: Treatment |
| Official Title: | The Effects of Compound Herbal Formula(TPE-1) for Leukopenia and Cancer-related Fatigue in Breast Cancer Patients With Radiotherapy |
- the % change of white blood cell(WBC) count [ Time Frame: 6 weeks ] [ Designated as safety issue: Yes ]WBC will be checked before taking TPE ans after taking TPE-1.
- Hemoglobin (Hb) [ Time Frame: 6 weeks ] [ Designated as safety issue: Yes ]The Hb will be checked before and after kaking TPE-1
| Estimated Enrollment: | 60 |
| Study Start Date: | May 2010 |
| Estimated Primary Completion Date: | April 2011 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Placebo Comparator: herbal A
dilute of (TPE-1) decoction.
|
Drug: Chinese herbal medicine decoction
100 ml /Qd for 6 weeks(42 days)
Other Name: TPE-1
|
|
Experimental: herbal B
TPE-1 decoction (100 ml)
|
Drug: Chinese herbal medicine decoction
100 ml /Qd for 6 weeks(42 days)
Other Name: TPE-1
|
Detailed Description:
TPE-1 is designed according to TCM concept. It is not anti-cancer directly, it is enhancing the Qi flow and immunity of breast cancer when they are just finishing chemotherapy and on going radiotherapy. Many Chinese population will seeking Chinese herbal medicine under the same condition.
Eligibility| Ages Eligible for Study: | 18 Years to 70 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- breast cancer
- age between 18 to 70 yrs
- finished chemotherapy (adriamycin ), will receiving radiotherapy
- Chinese population
- KP$ between 40-100
- ECOG < 2
- WBC >4X10(9)/L and Hb > 10g/dl
- Assigned informed concent.
Exclusion Criteria:
- receiving operation during 14 days
- blood transfusion during one month.
- ALT >100mg/dL
- Creatinine >2.0mg/dL
- Total bilirubin >2.0mg/dL
- Infection
- prolation
- Taking anti-seizure , psychological drugs or any drugs not suitable patients
- AIDS or any disease diagnosed by physician and not suitable patients.
Contacts and Locations| Contact: Chung-Hua Hsu, MD, PhD | 886-2-2388-7088 ext 3828 | owlherbs@yahoo.com.tw |
| Taiwan | |
| Shuang Ho Hospital | Recruiting |
| Taipei, Taiwan, 886 | |
| Contact: Chung-Hua Hsu, MD, PhD 886-2-2388-7088 ext 3828 owlherbs@yahoo.com.tw | |
| Principal Investigator: Chung-Hua Hsu, MD, PhD | |
More Information
No publications provided
| Responsible Party: | Chung-Hua Hsu, Taipei City Hospital |
| ClinicalTrials.gov Identifier: | NCT01142479 History of Changes |
| Other Study ID Numbers: | TPE-1-breast Ca |
| Study First Received: | June 10, 2010 |
| Last Updated: | June 10, 2010 |
| Health Authority: | Taiwan: Department of Health |
Keywords provided by Taipei City Hospital:
|
Breast Cancer Radiotherapy Chinese herbal medicine TPE-1 Leukopenia |
Additional relevant MeSH terms:
|
Breast Neoplasms Leukopenia Neoplasms by Site Neoplasms |
Breast Diseases Skin Diseases Leukocyte Disorders Hematologic Diseases |
ClinicalTrials.gov processed this record on May 23, 2013