Family Member Has History of Colorectal Adenoma of Adenocarcinoma Clinical Trial
Official title:
Effect of Folate on Colonic and Blood Cells
| Verified date | November 2013 |
| Source | Rockefeller University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | United States: Food and Drug Administration |
| Study type | Interventional |
This study looks at the effect of folate supplementation and depletion on the blood cells and the colorectal cells. To examine the effect of these changes, blood samples and colorectal biopsy samples are collected. The genetic material (RNA and DNA) is examined to see what changes occur during the depletion and supplementation of folate. The hypothesis is that folate may help prevent colon cancer
| Status | Completed |
| Enrollment | 20 |
| Est. completion date | September 2008 |
| Est. primary completion date | |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Both |
| Age group | 40 Years to 72 Years |
| Eligibility |
Inclusion Criteria: 1. Men or post-menopausal women ages 40 to 72 years old that have a personal history of colorectal adenomatous polyps and/or have a family history of colorectal cancer or polyps will be included. Women have to be =2 years post-menopause (2 years after the last menstrual period). 2. Ambulatory and in good health. - Exclusion Criteria: - 1. Personal history of cancer other than non-melanoma skin cancer. 2. History of hereditary non-polyposis colon cancer or more that one first degree family member with colorectal or endometrial cancers. 3. Diseases of the bowel such as intestinal malabsorption or inflammatory bowel disease 4. Surgery to the stomach or colon not including removal of the appendix or surgery to the esophagus (food tube) 5. Any excessive bleeding or clotting disorder or if you are taking blood thinners. 6. Abnormalities of or conditions predisposing you to abnormalities of, folate metabolism. 7. Untreated hyperthyroidism (increase in thyroid function) or insulin-requiring diabetes mellitus 8. Daily alcohol intake greater than 2 ½ shot glasses of whisky or three -8 ounce glasses of beer or wine. 9. No regular dosing of 660 mg of aspirin per day or more than 660 mg per day This is equal to or more than two tablets of 325 mg. of regular strength aspirin; or equal to or more than one tablet of 500 mg. extra-strength aspirin. You must not have regularly taken dosages of nonsteroidal anti-inflammatory agents (NSAID's) within the last 3 months. One example of an NSAID is ibuprofen. If you have been taking aspirin for heart or blood vessel protection regularly for at least one month before your first screening visit, you will remain on that same amount of medicine throughout the study and is allowed as follows: - Aspirin 1 to 2 regular aspirin tablets (325 mg per tablet) per day, or - Baby aspirin per day (81mg tablet). 10. A blood level (plasma) Vitamin B12 level less than 250pg/mL or a folate level greater than 20 ng/ml 11. A blood (plasma) homocysteine level equal to or greater than 17 µmol/L 12. Taking a medication called, sterol-binding resins, such as cholestyramine (Questran ®), which is for the treatment of high blood cholesterol. 13. Taking other investigational medications or multiple other medications that might, in the opinion of the investigator, alter cell production in your rectum; folate metabolism, or kidney or liver metabolism. 14. Any serious illness that would be anticipated to limit life expectancy to less than 6 months 15. Sustained elevated blood pressure greater than 150/95 mm Hg for three consecutive readings. 16. Clinically significant liver disease as evidenced by blood levels of alanine amniotransferase or aspartate amniotransferase, greater than two times the upper limits of the normal range, unexplained elevated alkaline phosphatase, or kidney disease with blood creatinine level greater than 2.0 mg/dL. 17. HIV positive test results. 18. Currently taking any of the following: - Weight control medications. - Folic acid containing medications greater than 400 micrograms per day. - Hormone replacement therapies or oral, transplanted, and injected contraceptives. - Thyroid hormone replacement medications o These will be only allowed if you have been stable on thyroid medication (euthyroid) for three months. - Medication interfering with the folic acid metabolic effects such as methotrexate (includes Folex® and Trexall® and others), antiepileptic drugs such as phenytoin (Dilantin®), phenobarbital, primidone or sulfonamides (includes some antimicrobial agents) and folinic acid derivatives (Leucovorin®). - Lipid-lowering medications (with the following exceptions) If you have been taking the following lipid lowering medication of the class called "statins" regularly for at least one month before your first screening visit, you will remain on the same amount of medicine throughout the study. - Atorvastatin (Lipitor©) 10 or 20 mg/day - Fluvastatin (Lescol©) 20 mg or 40 mg/day - Lovastatin (Levacor©) 10 or 20 mg/day - Pravastatin (Pravachol©) 10 or 20 mg/day - Simivastatin (Zocor©) 5 or 10 mg/day |
Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind, Primary Purpose: Prevention
| Country | Name | City | State |
|---|---|---|---|
| United States | Rockefeller University Hospital | New York | New York |
| Lead Sponsor | Collaborator |
|---|---|
| Rockefeller University |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Measurements of established folate-related endpoints in DNA from blood mononuclear cells and rectal cells: | |||
| Primary | Luracil incorporation in blood mononuclear cells | |||
| Primary | Strand breaks in the coding region of p53 in blood cells and rectal biopsy cells | |||
| Primary | DNA methylation (overall, p53, coding, p16 promotor. MLH1 promotor) in blood cells and rectal biopsy cells | |||
| Secondary | Measurements of differential gene expression in colonic and blood cells by microarray analysis, further defining folate's action in modifying cell cycle activity, cell maturation, signal transduction and oncogene expression. |