Clinical Trials Directory

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

TypeNameDescription
DRUGdi indolylmethane (DIM)This is the agent being studies. Similar agents have been reported to have potential activity.
DIETARY_SUPPLEMENTRed rice branthis 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.