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Omeprazole and Amoxicillin and/or Vitamin and Mineral Supplements and/or Garlic Supplements in Preventing Stomach Cancer in Patients With Precancerous Stomach Lesions - Article


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Cancer Alternative Therapy

Alternative Therapy for Cancer


Clinical Trial: Omeprazole and Amoxicillin and/or Vitamin and Mineral Supplements and/or Garlic Supplements in Preventing Stomach Cancer in Patients With Precancerous Stomach Lesions

This study is not yet open for patient recruitment.
Verified by National Cancer Institute (NCI) August 2005

Sponsored by: National Cancer Institute (NCI)
Information provided by: National Cancer Institute (NCI)
ClinicalTrials.gov Identifier: NCT00134121

Purpose

RATIONALE: Chemoprevention is the use of certain drugs or supplements to keep cancer from forming, growing, or coming back. The use of omeprazole and amoxicillin and/or vitamin and mineral supplements and/or garlic supplements may prevent stomach cancer.

PURPOSE: This randomized clinical trial is studying omeprazole and amoxicillin and/or vitamin and mineral supplements and/or garlic supplements to see how well they work in preventing stomach cancer in patients with precancerous stomach lesions.

Condition Intervention
Gastric Cancer
Precancerous Condition
 Drug: amoxicillin
 Drug: ascorbic acid
 Drug: beta carotene
 Drug: garlic
 Drug: omeprazole
 Drug: selenium
 Drug: vitamin E
 Procedure: antibiotic therapy
 Procedure: biologically based therapies
 Procedure: cancer prevention intervention
 Procedure: chemoprevention of cancer
 Procedure: complementary and alternative therapy
 Procedure: dietary intervention
 Procedure: infection prophylaxis/management
 Procedure: nutritional supplementation
 Procedure: proton pump inhibitor therapy
 Procedure: supportive care/therapy

MedlinePlus related topics:  Cancer;   Cancer Alternative Therapies;   Stomach Cancer

Study Type: Interventional
Study Design: Prevention

Official Title: Randomized Study of Omeprazole and Amoxicillin and/or Vitamin and Mineral Supplementation Comprising Beta Carotene, Vitamin E, Ascorbic Acid, and Selenium and/or Garlic Supplementation for the Prevention of Gastric Cancer in Patients With Precancerous Gastric Lesions

Further Study Details: 

OBJECTIVES:

Primary

Secondary

  • Compare the effects of these regimens on the rates of transition among the precancerous histopathologic states in these patients.
  • Compare the rate of Helicobacter pylori (H. pylori) eradication and reinfection in patients treated with these regimens.
  • Compare the effect of these regimens on blood pressure in these patients.

OUTLINE: This is a randomized, double-blind, placebo-controlled study. Patients are stratified according to Helicobacter pylori (H. pylori) antibody status (positive vs negative) and gender. Patients with an initial H. pylori infection are randomized to 1 of 8 treatment arms (I-VIII). Patients testing negative for H. pylori are randomized to 1 of 4 treatment arms (IX-XII).

After completion of study treatment, patients are followed at 3 months.

PROJECTED ACCRUAL: Approximately 3,600 patients (approximately 2,400 randomized to arms I-VIII [patients with Helicobacter pylori (H. pylori) infection] and 1,000 randomized to arms IX-XII [patients without H. pylori infection]) will be accrued for this study.

Eligibility

Ages Eligible for Study:  35 Years   -   69 Years,  Genders Eligible for Study:  Both
Criteria

DISEASE CHARACTERISTICS:

  • Histologically confirmed precancerous gastric lesions by gastroscopic examination
  • Gastroscopic results must have been obtained through prior participation in an endoscopic survey conducted in Lindqu, Shandong Province, China
  • At high risk for gastric cancer
  • Resident of Lindqu, Shandong Province, China

PATIENT CHARACTERISTICS:

Age

  • 35 to 69

Performance status

  • Not specified

Life expectancy

  • Not specified

Hematopoietic

  • No history of bleeding disorder

Hepatic

Renal

  • No renal disease

Cardiovascular

  • No heart failure

Pulmonary

  • No emphysema

Other

  • Not pregnant
  • No allergy to penicillin or similar drugs
  • No cancer except resected nonmelanoma skin cancer
  • No other life-threatening illness

PRIOR CONCURRENT THERAPY:

Biologic therapy

  • Not specified

Chemotherapy

  • Not specified

Endocrine therapy

  • Not specified

Radiotherapy

  • Not specified

Surgery

  • Not specified

Other

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00134121


Study chairs or principal investigators

Mitchel H. Gail, MD, PhD,  Study Chair,  National Cancer Institute (NCI)   

More Information

Clinical trial summary from the National Cancer Institute''''s PDQ® database

Study ID Numbers:  CDR0000437906; NCI-OH-95-C-N029; BICR-OH95-C-N029
Last Updated:  August 23, 2005
Record first received:  August 22, 2005
ClinicalTrials.gov Identifier:  NCT00134121
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-08-30


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Page Updated: September 6, 2005
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