Diindolylmethane in Treating Patients With Abnormal Cervical Cells
Primary Purpose
Cervical Cancer, Precancerous Condition
Status
Completed
Phase
Phase 3
Locations
United Kingdom
Study Type
Interventional
Intervention
oral microencapsulated diindolylmethane
polymerase chain reaction
cervical Papanicolaou test
cytology specimen collection procedure
colposcopic biopsy
Sponsored by
About this trial
This is an interventional prevention trial for Cervical Cancer focused on measuring cervical cancer, cervical intraepithelial neoplasia grade 2, cervical intraepithelial neoplasia grade 3, cervical intraepithelial neoplasia grade 1
Eligibility Criteria
DISEASE CHARACTERISTICS:
First mildly dyskaryotic Pap smear or a second borderline Pap smear taken within the Cervical Screening Wales program
- Patients under surveillance following treatment for high-grade cervical intraepithelial neoplasia are not eligible
- No clinical suspicion of a concurrent invasive cervical cancer
PATIENT CHARACTERISTICS:
- No invasive cancer within the past 3 years
- No known HIV positivity
- Not pregnant or nursing
- Not planning to become pregnant within the next 6 months
PRIOR CONCURRENT THERAPY:
- No concurrent immunosuppressive drugs, warfarin, or theophylline
- No concurrent proton pump inhibitor drugs for ulcer or reflux disease (i.e., rabeprazole, esomeprazole magnesium, lansoprazole, omeprazole, or pantoprazole sodium)
Sites / Locations
- Barts and the London School of Medicine
- University Hospital of Wales
Outcomes
Primary Outcome Measures
Biopsy confirmed high-grade cervical intraepithelial neoplasia (CIN) at 6 months
Secondary Outcome Measures
Change in lesion size at 6 months
Human papillomavirus (HPV) status and characteristics (type, viral load, and integration) at baseline and 6 months
Change in cervical cytology at 6 months
CIN ≥ grade 3 on histology at 6 months
Long term follow-up (i.e., 7 years)
Migraine, premenstrual syndrome (PMS), menstruation, and body weight
Full Information
NCT ID
NCT00462813
First Posted
April 18, 2007
Last Updated
August 6, 2013
Sponsor
Barts and the London School of Medicine and Dentistry
1. Study Identification
Unique Protocol Identification Number
NCT00462813
Brief Title
Diindolylmethane in Treating Patients With Abnormal Cervical Cells
Official Title
An Investigation Into the Effects of Diidolylmethane (BioResponse DIM®) Supplementation in Women With Low-Grade Cervical Cytological Abnormalities [CRISP-1]
Study Type
Interventional
2. Study Status
Record Verification Date
September 2008
Overall Recruitment Status
Completed
Study Start Date
October 2004 (undefined)
Primary Completion Date
June 2008 (Actual)
Study Completion Date
January 2010 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Barts and the London School of Medicine and Dentistry
4. Oversight
5. Study Description
Brief Summary
RATIONALE: Chemoprevention is the use of certain drugs to keep cancer from forming. The use of diindolylmethane, a substance found in cruciferous vegetables, may keep cervical intraepithelial neoplasia or cervical cancer from forming.
PURPOSE: This randomized phase III trial is studying diindolylmethane to see how well it works compared to a placebo in treating patients with abnormal cervical cells.
Detailed Description
OBJECTIVES:
Compare the effect of diindolylmethane vs placebo in reducing the prevalence of histologically proven high-grade cervical intraepithelial neoplasia in patients with low-grade cervical cytological abnormalities.
Compare the effect of these regimens in reducing the prevalence of cytological abnormalities in these patients.
Compare the effect of these regimens in changing the clinical appearance of the cervix in these patients.
Determine if diindolylmethane offers benefits in relation to human papillomavirus (HPV) status, including HPV type, viral load, and integration.
Determine the side effects of supplementation with diindolylmethane.
Determine the effects of this drug on migraine, mastalgia, weight, and premenstrual syndrome (PMS).
OUTLINE: This is a double-blind, randomized, placebo-controlled, multicenter study. Patients are randomized to 1 of 2 treatment arms.
Arm I: Patients receive oral diindolylmethane once daily for 6 months.
Arm II: Patients receive oral placebo once daily for 6 months. Patients undergo cervical sampling at baseline and at 6 months for Pap testing by liquid based cytology and human papillomavirus (HPV) testing by polymerase chain reaction. Some patients also undergo urine and hair sample collection at baseline and at 3 and 6 months. Samples are analyzed for estrogen and diindolylmethane metabolites, to monitor patient compliance and response to treatment. Some patients have a cervical photograph taken using a colposcope at baseline and at 6 months. All patients undergo colposcopy at 6 months.
Patients complete a questionnaire at baseline (i.e., for reproductive history, diet, smoking, and premenstrual symptoms) and at 6 months (i.e., for side effects, compliance, changes in smoking, and contraception use). Patients with moderate to severe premenstrual syndrome (PMS) also complete PMS questionnaires once monthly during months 1-6 and 4 months following completion of study therapy. All patients are instructed to maintain current diet and to keep cruciferous vegetables and soy products constant during study course.
After completion of study treatment, patients are followed periodically for up to 7 years.
PROJECTED ACCRUAL: A total of 3,000 patients will be accrued for this study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cervical Cancer, Precancerous Condition
Keywords
cervical cancer, cervical intraepithelial neoplasia grade 2, cervical intraepithelial neoplasia grade 3, cervical intraepithelial neoplasia grade 1
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 3
Masking
Double
Allocation
Randomized
Enrollment
3000 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
oral microencapsulated diindolylmethane
Intervention Type
Genetic
Intervention Name(s)
polymerase chain reaction
Intervention Type
Other
Intervention Name(s)
cervical Papanicolaou test
Intervention Type
Other
Intervention Name(s)
cytology specimen collection procedure
Intervention Type
Procedure
Intervention Name(s)
colposcopic biopsy
Primary Outcome Measure Information:
Title
Biopsy confirmed high-grade cervical intraepithelial neoplasia (CIN) at 6 months
Secondary Outcome Measure Information:
Title
Change in lesion size at 6 months
Title
Human papillomavirus (HPV) status and characteristics (type, viral load, and integration) at baseline and 6 months
Title
Change in cervical cytology at 6 months
Title
CIN ≥ grade 3 on histology at 6 months
Title
Long term follow-up (i.e., 7 years)
Title
Migraine, premenstrual syndrome (PMS), menstruation, and body weight
10. Eligibility
Sex
Female
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS:
First mildly dyskaryotic Pap smear or a second borderline Pap smear taken within the Cervical Screening Wales program
Patients under surveillance following treatment for high-grade cervical intraepithelial neoplasia are not eligible
No clinical suspicion of a concurrent invasive cervical cancer
PATIENT CHARACTERISTICS:
No invasive cancer within the past 3 years
No known HIV positivity
Not pregnant or nursing
Not planning to become pregnant within the next 6 months
PRIOR CONCURRENT THERAPY:
No concurrent immunosuppressive drugs, warfarin, or theophylline
No concurrent proton pump inhibitor drugs for ulcer or reflux disease (i.e., rabeprazole, esomeprazole magnesium, lansoprazole, omeprazole, or pantoprazole sodium)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter Sasieni, MD
Organizational Affiliation
Barts and the London School of Medicine and Dentistry
Official's Role
Study Chair
Facility Information:
Facility Name
Barts and the London School of Medicine
City
London
State/Province
England
ZIP/Postal Code
EC1M 6BQ
Country
United Kingdom
Facility Name
University Hospital of Wales
City
Cardiff
State/Province
Wales
ZIP/Postal Code
CF14 4XW
Country
United Kingdom
12. IPD Sharing Statement
Links:
URL
http://www.ncbi.nlm.nih.gov/pubmed/22075942
Description
Effect of diindolylmethane supplementation on low-grade cervical cytological abnormalities: double-blind, randomised, controlled trial. Br J Cancer. 2012 Jan 3;106(1):45-52. doi: 10.1038/bjc.2011.496. Epub 2011 Nov 10.
Learn more about this trial
Diindolylmethane in Treating Patients With Abnormal Cervical Cells
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