search
Back to results

Vitamin D/Calcium Polyp Prevention Study

Primary Purpose

Colorectal Cancer, Polyps, Adenomas

Status
Completed
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
Calcium Carbonate
Vitamin D3
placebo
Sponsored by
Dartmouth-Hitchcock Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Colorectal Cancer focused on measuring Colorectal neoplasms, Adenomatous polyps

Eligibility Criteria

45 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: One or more histologically verified neoplastic polyp (adenoma) that is at least 2 mm in size removed from the large bowel with the entire large bowel examined by colonoscopy and documented to be free of further polyps or areas suspicious for neoplasia within 120 days of study entry Anticipated colonoscopic follow-up three years or five years after the qualifying colonoscopy Age between 45 and 75 years at enrollment (Women)Agreement to avoid pregnancy (i.e., use of standard contraception) Willingness to forego calcium supplementation (including multivitamins containing calcium) or, for women only, option of taking calcium supplementation of 1200 mg/daily (contained in the study pills) Willingness to forego vitamin D supplementation (including multivitamins containing vitamin D) Agreement to daily dietary intake of the equivalent of not more than 1200 mg calcium Agreement to daily dietary intake of the equivalent of not more than 400 IU vitamin D Blood calcium level within normal range Blood creatinine level not to exceed 20% above upper limit of normal Serum 25-(OH)-vitamin D within lower limit of normal to 70 ng/ml Ability and willingness to follow the study protocol, as indicated by provision of informed consent to participate Good general health, with no severely debilitating diseases or active malignancy that might compromise the patient's ability to complete the study Exclusion Criteria: General exclusionary criteria: Participation in another colorectal (bowel) study (intervention study) in the past 5 years Current participation in any other clinical trial (intervention study) Pregnancy or lactation A diagnosis of narcotic or alcohol dependence in the past 5 years A diagnosis of dementia (e.g. Alzheimer's) in the past 5 years A diagnosis of a significant psychiatric disability (e.g. Schizophrenia, refractory bipolar disorder, current severe depression) in the past 5 years Exclusions due to derangement of calcium metabolism or indications /contraindications to study agents: Any diagnosis of kidney stones A diagnosis of granulomatous diseases, e.g. sarcoidosis, active chronic fungal or mycobacterial infections (tuberculosis, histoplasmosis, coccidioidomycosis, blastomycosis), berylliosis, Wegener's granulomatosis in the past 5 years A diagnosis of hyperparathyroidism or other serious disturbance of calcium metabolism in the past 5 years A diagnosis of severe kidney disease, e.g. chronic renal failure in the past 5 years A diagnosis of unexplained hypercalcemia in the past 5 years Any Diagnosis of osteoporosis with physician recommendation for treatment of low bone mass A diagnosis of two or more low trauma fractures in the past 5 years A diagnosis of a medical condition requiring treatment with vitamin D (e.g. osteomalacia) in the past 5 years Exclusions due to intestinal or bowel problems: Any diagnosis of invasive carcinoma of the large bowel (even if confined to a polyp) Any diagnosis of familial colorectal cancer syndromes, e.g. Familial Adenomatous Polyposis (FAP) (including Gardner syndrome, Turcot's syndrome), Hereditary Nonpolyposis Colorectal Cancer (HNPCC), Hamartomatous Polyposis syndromes (including Peutz-Jeghers or Familial Juvenile Polyposis) Any diagnosis of inflammatory bowel disease, e.g. Crohn's Disease, Ulcerative Colitis A diagnosis of chronic intestinal malabsorption syndromes, e.g. celiac sprue, bacterial overgrowth, chronic pancreatitis, pancreatic insufficiency in the past 5 years Any large bowel resection Exclusions due to poor health: A diagnosis of malignancy, other than non-melanoma skin cancer in the past 5 years A diagnosis of severe lung disease - class 3 or 4 (e.g. chronic obstructive pulmonary disease or emphysema requiring oxygen) in the past 5 years A diagnosis of severe heart disease: cardiovascular disease functional class 3 or 4 in the past 5 years Any diagnosis of severe liver disease, e.g. cirrhosis Exclusions due to shipping regulations: Any current/past HIV positive diagnosis Active hepatitis B, defined as : Hep B surface antigen positive Active hepatitis C, defined as : measurable hepatitis C RNA Drug exclusions: Use of chronic oral corticosteroid therapy in the past 5 years Use of lithium in the past 5 years Use of phenytoin's in the past 5 years Use of quinidine in the past 5 years Use of therapeutic vitamin D in the past 5 years

Sites / Locations

  • University of Southern California
  • University of Colorado
  • Emory University
  • University of Iowa
  • University of Minnesota
  • Dartmouth Hitchcock Medical Center
  • University of North Carolina
  • Cleveland Clinic Foundation
  • University of South Carolina
  • University of Texas
  • University of Puerto Rico

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Arm Label

Full Factorial Placebo

Full Factorial Calcium

Full Factorial Vitamin D

Full Factorial Calcium Plus Vitamin D

Two Arm Placebo

Two Arm Vitamin D

Arm Description

subjects in 2X2 factorial design; randomized to daily placebo

subjects in 2X2 factorial design; randomized to daily 1200 mg as calcium carbonate

Subjects in 2X2 factorial design; randomized to daily 1000 IU vitamin D3

Subjects in 2X2 factorial design; randomized to daily 1200 mg as calcium carbonate and 1000 IU vitamin D3

Women choosing to take daily 1200 mg as calcium carbonate randomized to daily placebo

Women choosing to take daily 1200 mg as calcium carbonate randomized to daily 1000 IU vitamin D3

Outcomes

Primary Outcome Measures

Colorectal Adenomas

Secondary Outcome Measures

Advanced Colorectal Lesions
Includes: adenomas >=1 cm, adenomas with high grade dysplasia, adenomas with villous features, or cancer.

Full Information

First Posted
September 7, 2005
Last Updated
February 6, 2017
Sponsor
Dartmouth-Hitchcock Medical Center
Collaborators
National Cancer Institute (NCI)
search

1. Study Identification

Unique Protocol Identification Number
NCT00153816
Brief Title
Vitamin D/Calcium Polyp Prevention Study
Official Title
Vitamin D/Calcium Polyp Prevention Study
Study Type
Interventional

2. Study Status

Record Verification Date
February 2017
Overall Recruitment Status
Completed
Study Start Date
July 2004 (Actual)
Primary Completion Date
October 2013 (Actual)
Study Completion Date
June 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Dartmouth-Hitchcock Medical Center
Collaborators
National Cancer Institute (NCI)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Extensive experimental and observational data suggest that intake of calcium and of vitamin D exert protective effects on colorectal neoplasia. Building on their previous work, the investigators will investigate the chemopreventive effect of vitamin D in the large bowel, to study whether calcium with vitamin D is more effective than calcium alone, and to confirm their positive finding regarding calcium. The goal of this study is the development of chemopreventive combinations that will reduce risk of colorectal neoplasia sufficiently to permit the lengthening of surveillance intervals in most patients and to clarify important issues regarding the mechanisms of colorectal carcinogenesis and chemoprevention.
Detailed Description
This study is a double-blind, placebo-controlled trial of vitamin D and/or calcium supplementation for the prevention of large bowel adenomas. Subjects will be recruited from 11 Study Centers in North America. Eligible subjects will have had at least one large bowel adenoma removed in the 4 months prior to study entry and no remaining polyps in the bowel after complete colonoscopic examination. Participants will be randomized in a partial 2 x 2 factorial design to vitamin D (1000 IU/day), calcium carbonate (1200 mg elemental calcium/day), both agents, or placebo only (Full Factorial randomization). Women who decline to forego calcium supplementation will be randomized only to calcium alone or to calcium plus vitamin D (Two Arm randomization). Randomization will be stratified by gender, study center of recruitment, and anticipated follow-up interval (see below), and will be conducted separately for female subjects randomized only to vitamin D. We anticipate enrolling up to 3000 participants to reach a total of up to 2400 randomized subjects. As safety measures, blood levels of calcium, creatinine, and 25-(OH)-vitamin D will be obtained at baseline and 1 year after randomization, as well as 3 years after randomization for subjects with a 5-year surveillance cycle. Every six months after randomization subjects will complete a questionnaire regarding compliance with study agents, use of medications and vitamin/mineral supplements, illnesses, hospitalizations, and dietary intake of calcium and vitamin D. The primary endpoint of the study will be new adenomas detected on follow-up colonoscopy. These examinations are scheduled to occur either 3 years or 5 years after the qualifying examination, depending on the follow-up interval recommended by each patient's endoscopist. Some patients may, for medical reasons, have a colonoscopy at a time other than 3 or 5 years after the qualifying examination. Information from these exams will be included in analyses where appropriate. In the primary analyses, the occurrence of new adenomas in the interval between randomization and the follow-up exam will be compared between subjects randomized to vitamin D (with or without calcium) versus those randomized to no vitamin D (with or without calcium), between subjects randomized to calcium (with or without vitamin D) versus those randomized to no calcium (with or without vitamin D; excluding women electing to receive calcium who therefore cannot participate in the calcium component of the study), and between those randomized to calcium plus vitamin D versus those randomized to calcium alone. In secondary analyses, we will examine the impact of baseline vitamin D levels and vitamin D receptor (VDR) polymorphisms on the vitamin D effects. Effects on advanced adenomas will also be assessed as a secondary outcome. Participants will be invited to participate in an optional Observational Follow Up phase of the study that will begin following the end of treatment. In this phase of the study, subjects will continue to be followed on an observational basis (no study treatment) with annual questionnaires until the time of a subsequent colonoscopy that is at least three years from the follow up colonoscopy at which study treatment was ended. We will examine the occurrence of new adenomas in the interval between the colonoscopy exam at the end of study treatment and the exam at the end of observational follow up period.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer, Polyps, Adenomas
Keywords
Colorectal neoplasms, Adenomatous polyps

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2, Phase 3
Interventional Study Model
Factorial Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
2813 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Full Factorial Placebo
Arm Type
Experimental
Arm Description
subjects in 2X2 factorial design; randomized to daily placebo
Arm Title
Full Factorial Calcium
Arm Type
Experimental
Arm Description
subjects in 2X2 factorial design; randomized to daily 1200 mg as calcium carbonate
Arm Title
Full Factorial Vitamin D
Arm Type
Experimental
Arm Description
Subjects in 2X2 factorial design; randomized to daily 1000 IU vitamin D3
Arm Title
Full Factorial Calcium Plus Vitamin D
Arm Type
Experimental
Arm Description
Subjects in 2X2 factorial design; randomized to daily 1200 mg as calcium carbonate and 1000 IU vitamin D3
Arm Title
Two Arm Placebo
Arm Type
Experimental
Arm Description
Women choosing to take daily 1200 mg as calcium carbonate randomized to daily placebo
Arm Title
Two Arm Vitamin D
Arm Type
Experimental
Arm Description
Women choosing to take daily 1200 mg as calcium carbonate randomized to daily 1000 IU vitamin D3
Intervention Type
Drug
Intervention Name(s)
Calcium Carbonate
Intervention Description
3 gm/daily; 1200 mg elemental calcium/daily; two tablets per day; 600 mg elemental calcium/tablet
Intervention Type
Drug
Intervention Name(s)
Vitamin D3
Intervention Description
1000 IU/daily; two tablets per day; 500 IU per tablet
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
placebo; two tablets per day
Primary Outcome Measure Information:
Title
Colorectal Adenomas
Time Frame
1 to 10 years
Secondary Outcome Measure Information:
Title
Advanced Colorectal Lesions
Description
Includes: adenomas >=1 cm, adenomas with high grade dysplasia, adenomas with villous features, or cancer.
Time Frame
1 to 10 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: One or more histologically verified neoplastic polyp (adenoma) that is at least 2 mm in size removed from the large bowel with the entire large bowel examined by colonoscopy and documented to be free of further polyps or areas suspicious for neoplasia within 120 days of study entry Anticipated colonoscopic follow-up three years or five years after the qualifying colonoscopy Age between 45 and 75 years at enrollment (Women)Agreement to avoid pregnancy (i.e., use of standard contraception) Willingness to forego calcium supplementation (including multivitamins containing calcium) or, for women only, option of taking calcium supplementation of 1200 mg/daily (contained in the study pills) Willingness to forego vitamin D supplementation (including multivitamins containing vitamin D) Agreement to daily dietary intake of the equivalent of not more than 1200 mg calcium Agreement to daily dietary intake of the equivalent of not more than 400 IU vitamin D Blood calcium level within normal range Blood creatinine level not to exceed 20% above upper limit of normal Serum 25-(OH)-vitamin D within lower limit of normal to 70 ng/ml Ability and willingness to follow the study protocol, as indicated by provision of informed consent to participate Good general health, with no severely debilitating diseases or active malignancy that might compromise the patient's ability to complete the study Exclusion Criteria: General exclusionary criteria: Participation in another colorectal (bowel) study (intervention study) in the past 5 years Current participation in any other clinical trial (intervention study) Pregnancy or lactation A diagnosis of narcotic or alcohol dependence in the past 5 years A diagnosis of dementia (e.g. Alzheimer's) in the past 5 years A diagnosis of a significant psychiatric disability (e.g. Schizophrenia, refractory bipolar disorder, current severe depression) in the past 5 years Exclusions due to derangement of calcium metabolism or indications /contraindications to study agents: Any diagnosis of kidney stones A diagnosis of granulomatous diseases, e.g. sarcoidosis, active chronic fungal or mycobacterial infections (tuberculosis, histoplasmosis, coccidioidomycosis, blastomycosis), berylliosis, Wegener's granulomatosis in the past 5 years A diagnosis of hyperparathyroidism or other serious disturbance of calcium metabolism in the past 5 years A diagnosis of severe kidney disease, e.g. chronic renal failure in the past 5 years A diagnosis of unexplained hypercalcemia in the past 5 years Any Diagnosis of osteoporosis with physician recommendation for treatment of low bone mass A diagnosis of two or more low trauma fractures in the past 5 years A diagnosis of a medical condition requiring treatment with vitamin D (e.g. osteomalacia) in the past 5 years Exclusions due to intestinal or bowel problems: Any diagnosis of invasive carcinoma of the large bowel (even if confined to a polyp) Any diagnosis of familial colorectal cancer syndromes, e.g. Familial Adenomatous Polyposis (FAP) (including Gardner syndrome, Turcot's syndrome), Hereditary Nonpolyposis Colorectal Cancer (HNPCC), Hamartomatous Polyposis syndromes (including Peutz-Jeghers or Familial Juvenile Polyposis) Any diagnosis of inflammatory bowel disease, e.g. Crohn's Disease, Ulcerative Colitis A diagnosis of chronic intestinal malabsorption syndromes, e.g. celiac sprue, bacterial overgrowth, chronic pancreatitis, pancreatic insufficiency in the past 5 years Any large bowel resection Exclusions due to poor health: A diagnosis of malignancy, other than non-melanoma skin cancer in the past 5 years A diagnosis of severe lung disease - class 3 or 4 (e.g. chronic obstructive pulmonary disease or emphysema requiring oxygen) in the past 5 years A diagnosis of severe heart disease: cardiovascular disease functional class 3 or 4 in the past 5 years Any diagnosis of severe liver disease, e.g. cirrhosis Exclusions due to shipping regulations: Any current/past HIV positive diagnosis Active hepatitis B, defined as : Hep B surface antigen positive Active hepatitis C, defined as : measurable hepatitis C RNA Drug exclusions: Use of chronic oral corticosteroid therapy in the past 5 years Use of lithium in the past 5 years Use of phenytoin's in the past 5 years Use of quinidine in the past 5 years Use of therapeutic vitamin D in the past 5 years
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John A. Baron, MD
Organizational Affiliation
Dartmouth-Hitchcock Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Southern California
City
Los Angeles
State/Province
California
ZIP/Postal Code
90089
Country
United States
Facility Name
University of Colorado
City
Denver
State/Province
Colorado
ZIP/Postal Code
80220
Country
United States
Facility Name
Emory University
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States
Facility Name
University of Iowa
City
Iowa City
State/Province
Iowa
ZIP/Postal Code
52242
Country
United States
Facility Name
University of Minnesota
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55455
Country
United States
Facility Name
Dartmouth Hitchcock Medical Center
City
Lebanon
State/Province
New Hampshire
ZIP/Postal Code
03766
Country
United States
Facility Name
University of North Carolina
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599
Country
United States
Facility Name
Cleveland Clinic Foundation
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States
Facility Name
University of South Carolina
City
Columbia
State/Province
South Carolina
ZIP/Postal Code
29203
Country
United States
Facility Name
University of Texas
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
University of Puerto Rico
City
San Juan
Country
Puerto Rico

12. IPD Sharing Statement

Citations:
PubMed Identifier
34289971
Citation
Passarelli MN, Mott LA, Barry EL, Rees JR, Baron JA. Oral Antibiotics and Risk of New Colorectal Adenomas During Surveillance Follow-up. Cancer Epidemiol Biomarkers Prev. 2021 Oct;30(10):1974-1976. doi: 10.1158/1055-9965.EPI-21-0323. Epub 2021 Jul 21.
Results Reference
derived
PubMed Identifier
33022713
Citation
Passarelli MN, Karagas MR, Mott LA, Rees JR, Barry EL, Baron JA. Risk of keratinocyte carcinomas with vitamin D and calcium supplementation: a secondary analysis of a randomized clinical trial. Am J Clin Nutr. 2020 Dec 10;112(6):1532-1539. doi: 10.1093/ajcn/nqaa267.
Results Reference
derived
PubMed Identifier
29496722
Citation
Crockett SD, Barry EL, Mott LA, Ahnen DJ, Robertson DJ, Anderson JC, Wallace K, Burke CA, Bresalier RS, Figueiredo JC, Snover DC, Baron JA. Calcium and vitamin D supplementation and increased risk of serrated polyps: results from a randomised clinical trial. Gut. 2019 Mar;68(3):475-486. doi: 10.1136/gutjnl-2017-315242. Epub 2018 Mar 1.
Results Reference
derived
PubMed Identifier
28767463
Citation
Anderson JC, Morris CB, Robertson DJ, Barry ELR, Figueiredo JC, Cruz-Correa M, Bostick RM, Ahnen DJ, Baron JA. Can the Sum of Adenoma Diameters (Adenoma Bulk) on Index Examination Predict Risk of Metachronous Advanced Neoplasia? J Clin Gastroenterol. 2018 Aug;52(7):628-634. doi: 10.1097/MCG.0000000000000899.
Results Reference
derived
PubMed Identifier
27978548
Citation
Barry EL, Peacock JL, Rees JR, Bostick RM, Robertson DJ, Bresalier RS, Baron JA. Vitamin D Receptor Genotype, Vitamin D3 Supplementation, and Risk of Colorectal Adenomas: A Randomized Clinical Trial. JAMA Oncol. 2017 May 1;3(5):628-635. doi: 10.1001/jamaoncol.2016.5917.
Results Reference
derived
PubMed Identifier
27683872
Citation
Rees JR, Mott LA, Barry EL, Baron JA, Bostick RM, Figueiredo JC, Bresalier RS, Robertson DJ, Peacock JL. Lifestyle and Other Factors Explain One-Half of the Variability in the Serum 25-Hydroxyvitamin D Response to Cholecalciferol Supplementation in Healthy Adults. J Nutr. 2016 Nov;146(11):2312-2324. doi: 10.3945/jn.116.236323. Epub 2016 Sep 28.
Results Reference
derived
PubMed Identifier
27474021
Citation
Rees JR, Mott LA, Barry EL, Baron JA, Figueiredo JC, Robertson DJ, Bresalier RS, Peacock JL. Randomized controlled trials: who fails run-in? Trials. 2016 Jul 29;17:374. doi: 10.1186/s13063-016-1451-9.
Results Reference
derived
PubMed Identifier
26465985
Citation
Baron JA, Barry EL, Mott LA, Rees JR, Sandler RS, Snover DC, Bostick RM, Ivanova A, Cole BF, Ahnen DJ, Beck GJ, Bresalier RS, Burke CA, Church TR, Cruz-Correa M, Figueiredo JC, Goodman M, Kim AS, Robertson DJ, Rothstein R, Shaukat A, Seabrook ME, Summers RW. A Trial of Calcium and Vitamin D for the Prevention of Colorectal Adenomas. N Engl J Med. 2015 Oct 15;373(16):1519-30. doi: 10.1056/NEJMoa1500409.
Results Reference
derived
PubMed Identifier
25329821
Citation
Barry EL, Mott LA, Melamed ML, Rees JR, Ivanova A, Sandler RS, Ahnen DJ, Bresalier RS, Summers RW, Bostick RM, Baron JA. Calcium supplementation increases blood creatinine concentration in a randomized controlled trial. PLoS One. 2014 Oct 15;9(10):e108094. doi: 10.1371/journal.pone.0108094. eCollection 2014.
Results Reference
derived
PubMed Identifier
25070320
Citation
Barry EL, Rees JR, Peacock JL, Mott LA, Amos CI, Bostick RM, Figueiredo JC, Ahnen DJ, Bresalier RS, Burke CA, Baron JA. Genetic variants in CYP2R1, CYP24A1, and VDR modify the efficacy of vitamin D3 supplementation for increasing serum 25-hydroxyvitamin D levels in a randomized controlled trial. J Clin Endocrinol Metab. 2014 Oct;99(10):E2133-7. doi: 10.1210/jc.2014-1389. Epub 2014 Jul 29.
Results Reference
derived
PubMed Identifier
24014734
Citation
Rees JR, Hendricks K, Barry EL, Peacock JL, Mott LA, Sandler RS, Bresalier RS, Goodman M, Bostick RM, Baron JA. Vitamin D3 supplementation and upper respiratory tract infections in a randomized, controlled trial. Clin Infect Dis. 2013 Nov;57(10):1384-92. doi: 10.1093/cid/cit549. Epub 2013 Sep 6.
Results Reference
derived
PubMed Identifier
18541589
Citation
Bischoff-Ferrari HA, Rees JR, Grau MV, Barry E, Gui J, Baron JA. Effect of calcium supplementation on fracture risk: a double-blind randomized controlled trial. Am J Clin Nutr. 2008 Jun;87(6):1945-51. doi: 10.1093/ajcn/87.6.1945.
Results Reference
derived

Learn more about this trial

Vitamin D/Calcium Polyp Prevention Study

We'll reach out to this number within 24 hrs