Folic Acid in Preventing Colorectal Polyps in Patients With Previous Colorectal Polyps

The recruitment status of this study is unknown because the information has not been verified recently.
Verified December 2009 by National Cancer Institute (NCI).
Recruitment status was  Active, not recruiting
Sponsor:
Collaborator:
Information provided by:
National Cancer Institute (NCI)
ClinicalTrials.gov Identifier:
NCT00512850
First received: August 6, 2007
Last updated: December 22, 2009
Last verified: December 2009

August 6, 2007
December 22, 2009
Not Provided
Not Provided
Diagnosis of a recurrent adenomatous polyp(s) of the colorectum on subsequent colonoscopy [ Designated as safety issue: No ]
Diagnosis of a recurrent adenomatous polyp(s) of the colorectum on subsequent colonoscopy
Complete list of historical versions of study NCT00512850 on ClinicalTrials.gov Archive Site
  • Number of adenomas per patient and the size and histology of these adenomas [ Designated as safety issue: No ]
  • Interaction between folic acid intake and alcohol, methionine, and aspirin intake [ Designated as safety issue: No ]
  • Number of adenomas per patient and the size of these adenomas
  • Interaction between folic acid intake and alcohol, methionine, and aspirin intake
Not Provided
Not Provided
 
Folic Acid in Preventing Colorectal Polyps in Patients With Previous Colorectal Polyps
Polyp Prevention Trial

RATIONALE: Chemoprevention is the use of certain substances to keep cancer from forming. The use of folic acid may prevent colorectal cancer.

PURPOSE: This randomized clinical trial is studying how well folic acid works compared with a placebo in preventing colorectal polyps in patients who have had previous colorectal polyps.

OBJECTIVES:

Primary

  • Determine if folic acid supplementation lowers the adenoma recurrence rate.

Secondary

  • Determine the number of adenomas per patient and the size and histology of the adenoma.
  • Assess the interaction between folic acid and alcohol, methionine, and aspirin intake.
  • Assess the interaction between folic acid and pretrial and midtrial folate levels.
  • Assess other complementary biomarkers such as DNA methylation and blood folate level as risk factors for polyp recurrence.

OUTLINE: Patients are randomized to 1 of 2 treatment arms.

  • Arm I: Patients receive oral folic acid once daily.
  • Arm II: Patients receive oral placebo once daily. At least 1 year after beginning treatment, patients are sent a blood collection kit in order to measure plasma vitamin B12 levels, to measure folate to assess compliance.
Interventional
Not Provided
Allocation: Randomized
Primary Purpose: Prevention
Colorectal Cancer
  • Dietary Supplement: folic acid
  • Genetic: DNA methylation analysis
Not Provided
Wu K, Platz EA, Willett WC, Fuchs CS, Selhub J, Rosner BA, Hunter DJ, Giovannucci E. A randomized trial on folic acid supplementation and risk of recurrent colorectal adenoma. Am J Clin Nutr. 2009 Dec;90(6):1623-31. Epub 2009 Oct 28.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
1000
Not Provided
Not Provided

DISEASE CHARACTERISTICS:

Inclusion criteria:

  • Participated in the Nurses' Health Study (NHS I) or the Health Professionals Follow-Up Study (HPFS) and have had a previous confirmed diagnosis of adenomatous polyp of the colon or rectum
  • Plan on having an endoscopy within 4 years after initiation of the trial
  • Must release medical records regarding past and any future endoscopies

PATIENT CHARACTERISTICS:

Inclusion criteria:

  • Plasma vitamin B12 concentration of ≥ 300 pg/mL or have a vitamin B12 concentration between 200 and 299 pg/mL and a methylmalonic acid (MMA) level ≤ 32 µg/L

Exclusion criteria:

  • Diagnosis of cancer other than non-melanoma skin cancer, or early stage breast or prostate cancer
  • Diagnosis of homocystinemia
  • Diagnosis of pernicious anemia
  • Any gastrointestinal disorder that could lead to a vitamin B12 deficiency
  • Diagnosis of cirrhosis or pancreatitis
  • Diagnosis of epilepsy, Alzheimer's disease, Parkinsonism, and psychiatric disorders that may interfere with normal functioning

PRIOR CONCURRENT THERAPY:

Exclusion criteria:

  • No prior gastrectomy, total colectomy, or pancreatectomy
  • Other concurrent multivitamins or supplements that contain folic acid (they may take specific supplements, such as A, C, E, calcium, and iron, or antioxidant formula vitamins)
  • No concurrent methotrexate or anticonvulsant
Both
up to 75 Years
No
Contact information is only displayed when the study is recruiting subjects
Not Provided
 
NCT00512850
CDR0000559650, BWH-1999-P-001674/10, BWH-94-06819
Not Provided
Not Provided
Dana-Farber/Brigham and Women's Cancer Center
National Cancer Institute (NCI)
Principal Investigator: Edward L. Giovannucci, MD, ScD Dana-Farber/Brigham and Women's Cancer Center
National Cancer Institute (NCI)
December 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP