Cancers Treated With Combination of Antrodia Cinnamomea and Chemotherapy

The recruitment status of this study is unknown because the information has not been verified recently.
Verified January 2011 by Chang Gung Memorial Hospital.
Recruitment status was  Recruiting
Sponsor:
Collaborator:
New Bellus Enterprises
Information provided by:
Chang Gung Memorial Hospital
ClinicalTrials.gov Identifier:
NCT01287286
First received: January 30, 2011
Last updated: February 6, 2011
Last verified: January 2011
  Purpose

The purpose of this study is to investigate if food supplements,Antrodia cinnamomea, could minimize the gastrointestinal symptom of cancer patients with chemotherapy.


Condition Intervention Phase
Neoplasm
Functional Gastrointestinal Disorder
Dietary Supplement: AC-Can
Dietary Supplement: placebo
Phase 2
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Double Blind (Subject, Caregiver, Investigator)
Primary Purpose: Treatment
Official Title: Cancers Treated With Combination of Antrodia Cinnamomea and Chemotherapy— a Double Blinded, Randomized, Placebo-controlled Trial

Resource links provided by NLM:


Further study details as provided by Chang Gung Memorial Hospital:

Primary Outcome Measures:
  • Gastrointestinal symptoms in case group reduces 10% than control group during chemotherapy. [ Time Frame: 1 month ] [ Designated as safety issue: No ]
    Post-chemotherapy nausea, vomiting and epigastragia, etc. including gastrointestinal symptom/sign without mention above.


Secondary Outcome Measures:
  • Life quality estimates of 10% improvement than control group. [ Time Frame: 3 months ] [ Designated as safety issue: No ]
    Life science related questionnairs visit 4 times just before treatment, after intervention 7 days, 30 days and 90 days.


Estimated Enrollment: 64
Study Start Date: June 2010
Estimated Study Completion Date: May 2012
Estimated Primary Completion Date: April 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: AC-Can
Antrodia cinnamomea and concomitant chemotherapy
Dietary Supplement: AC-Can
Antrodia cinnamomea compounds of 15 milliliters liquid per pack, oral post meal, twice in a day for 30 days
Other Name: AC
Placebo Comparator: control
Placebo and concomitant chemotherapy
Dietary Supplement: placebo
Placebo of 15 milliliters liquid per pack, oral post meal, twice in a day for 30 days
Other Name: Placebo

Detailed Description:

In our unpublished report shows that patients who took Antrodia Cinnamomea compound of 15 milliliters liquid twice in a day, might help white blood cells, red blood cells and hemoglobin increase after 2 months; liver glutamic pyruvic transaminase(GPT) index mitigation, P <0.05 difference statistically; In addition, liver glutamate oxaloacetate transaminase(GOT) and biochemical index of renal function had no abnormal data statistically. However, cancer patients with gastrointestinal disorders after chemotherapy is known to be a common side effect, we seek to investigate if Antrodia Cinnamomea improves the function of gastrointestinal system.

  Eligibility

Ages Eligible for Study:   18 Years to 80 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Histologically or cytologically confirmed Cancer.
  • Age ≦ 80 years old and ≧ 18 years old.
  • Eastern Cooperative Oncology Group(ECOG) performance status of 0-2.
  • Adequate organ function, including followings Hepatic: Total bilirubin level ≦1.5 x UNL, GOT and GPT ≦ 2.5 x UNL if no liver metastasis; GOT and GPT ≦ 5 x UNL if liver metastasis. Renal: Creatinine level< 1.5 milligram per deciliter or Estimated creatinine clearance(CCr) ≧ 60 milliliter per minute (CCr is estimated by Cockcroft-Gault formula, as appendix II)
  • Estimated life expectancy of at least 12 weeks.
  • Written(signed) Informed Consent
  • Ever treated and poor tolerance with platinum-based or anthracycline- based regimen, likely nausea and vomiting.

Exclusion Criteria:

  • Prior participation in any investigational drug study within 28 days
  • Active uncontrolled infections or human immunodeficiency virus(HIV) infection
  • Significant concurrent medical diseases, such as congestive heart failure, unstable angina, acute or recent myocardial infarction( 6 months before randomization), chronic obstructive pulmonary disease with frequent exacerbation, chronic renal diseases (estimated CCr 60 milliliter per minute), uncontrolled diabetes, uncontrolled hypertension, recent cerebrovascular disease episode( 6 months before randomization )
  • With clinically significant Gastrointestinal disorder (e.g. bleeding, inflammation, obstruction or diarrhea)
  • Psychiatric disorders that would compromise the patient's compliance or decision.
  • Pregnancy or breast feeding.
  • Known hypersensitivity to the component of investigational drugs.
  • Known or suspected Gilbert's syndrome
  • Poor compliance
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01287286

Contacts
Contact: Hsien-Hsueh E Chiu, MD +887-7-7317123 ext 2332 elley@adm.cgmh.org.tw

Locations
Taiwan
Division of Haematology and Oncology, Department of Internal Medicine and Traditional Chinese Medicine, Chang Gung Memorial Hospital - Kaohsiung Medical Center Recruiting
Niaosong, Kaohsiung, Taiwan, 83301
Contact: Pey-Harn Ywi-Chi, Bachelor    +886-7-7317123 ext 2332    kangta614@hotmail.com   
Contact: Kun-Ming Rau, MD    +886-7-7317123 ext 8303    kmrau58@adm.cgmh.org.tw   
Sub-Investigator: Hsien-Hsueh E Chiu, MD         
Sub-Investigator: Kun-Ming Rau, MD         
Sponsors and Collaborators
Chang Gung Memorial Hospital
New Bellus Enterprises
Investigators
Principal Investigator: Yu-Chiang Hung, MD, PhD Department of Traditional Chinese Medicine, Chang Gung Memorial Hospital - Kaohsiung Medical Center
  More Information

No publications provided

Responsible Party: Yu-Chiang Hung / MD, PhD, Department of Traditional Chinese Medicine, Chang Gung Memorial Hospital- Kaohsiung Medical Center
ClinicalTrials.gov Identifier: NCT01287286     History of Changes
Other Study ID Numbers: XMRPG890251
Study First Received: January 30, 2011
Last Updated: February 6, 2011
Health Authority: Taiwan: Department of Health

Keywords provided by Chang Gung Memorial Hospital:
Cancers
Antrodia cinnamomea
Chemotherapy
Gastrointestinal Disorder

Additional relevant MeSH terms:
Neoplasms
Digestive System Diseases
Gastrointestinal Diseases

ClinicalTrials.gov processed this record on August 21, 2014