Trial · NCT00462813
Diindolylmethane in Treating Patients With Abnormal Cervical Cells
NCT00462813, Phase 3, Completed, Barts and the London School of Medicine and Dentistry
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Diindolylmethane in Treating Patients With Abnormal Cervical Cells. Trials, record NCT00462813. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00462813
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Diindolylmethane in Treating Patients With Abnormal Cervical Cells
- NCT number
- NCT00462813
- Status
- Completed
- Phases
- Phase 3
- Enrollment
- 3,000 participants, estimated
- Lead sponsor
- Barts and the London School of Medicine and Dentistry
- Conditions
- Cervical Cancer, Precancerous Condition
- Interventions
- oral microencapsulated diindolylmethane, polymerase chain reaction, cervical Papanicolaou test, cytology specimen collection procedure, colposcopic biopsy
- First posted
- 2007-04-19
- Last updated
- 2013-08-07
- Other registries' IDs
- isrctn:ISRCTN47437431
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Biopsy confirmed high-grade cervical intraepithelial neoplasia (CIN) at 6 months | ||
| Secondary | Change in lesion size at 6 months | ||
| Secondary | Human papillomavirus (HPV) status and characteristics (type, viral load, and integration) at baseline and 6 months | ||
| Secondary | Change in cervical cytology at 6 months | ||
| Secondary | CIN ≥ grade 3 on histology at 6 months | ||
| Secondary | Long term follow-up (i.e., 7 years) | ||
| Secondary | Migraine, premenstrual syndrome (PMS), menstruation, and body weight |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT00462813
GET https://conductscience.org/api/trials/v1/NCT00462813/registered