Trials / Completed
CompletedNCT00212381
Oral Diindolylmethane (DIM) for the Treatment of Cervical Dysplasia
Diindolylmethane (DIM) Dietary Supplementation: A Nonsurgical Treatment for Cervical Intraepithelial Neoplasia (CIN)
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 62 (estimated)
- Sponsor
- New York Presbyterian Hospital · Academic / Other
- Sex
- Female
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Accepted
Summary
To determine if the use of oral Diindolylmethante (DIM), a marketed cruciferous vegetable based dietary supplement (Bioresponse-DIM), is associated with the regression of cervical dysplasia in otherwise healthy women.
Detailed description
To determine if the use of oral Diindolylmethane (DIM), a marketed cruciferous vegetable based dietary supplement (BioResponse-DIM®), is associated with the regression of cervical dysplasia in otherwise healthy women. Additionally, the study aims to see how the use of the BioResponse-DIM supplement correlates with cervical HPV colonization, and to asses the tolerability of daily DIM supplementation
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | di indolylmethane (DIM) | This is the agent being studies. Similar agents have been reported to have potential activity. |
| DIETARY_SUPPLEMENT | Red rice bran | this will act as the active comparator. The sponsor provided this as the "placebo" arm since it is a filler component of their DIM capsules |
Timeline
- Start date
- 2000-09-01
- Primary completion
- 2006-01-01
- Completion
- 2010-07-01
- First posted
- 2005-09-21
- Last updated
- 2017-03-29
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00212381. Inclusion in this directory is not an endorsement.