CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 90 enrolled
Drug / intervention
Imiquimod +1 moredrug
Likely dose
Not stated in record
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Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03233412
NCT03233412Phase 2Completed

Ensaio clínico Randomizado Avaliando a eficácia do Tratamento tópico Com Imiquimode em lesões Intraepiteliais Cervicais de Alto Grau

Barretos Cancer Hospital·interventional·Posted Jul 28, 2017·Updated Feb 17, 2021

In Brief

A Phase 2 clinical trial evaluating Control and Imiquimod for High Grade Intraepithelial Neoplasia and Cervix Cancer. Completed, enrolled 90 participants across 1 site.

Detailed Summary

Cervical cancer is one of the leading malignancies affecting women, with 311,000 deaths in 2018, most of them seen in underdeveloped countries. This neoplasm has a pre-invasive state, such as cervical intraepithelial neoplasia (CIN), which is caused by HPV (Human Papillomavirus) infection. The female organism most often is able to eliminate the virus, especially in young patients. However, when the infection becomes persistent, especially for subtypes 16 and 18, the risk of CIN developing an increased. Cytological screening programs can efficiently and wirelessly do this. As high-grade intraepithelial lesions (CIN 2/3) are as demonstrated by worse regression rate, only 13.3% at one year, and higher risk for progression to invasive cancer. As CIN 2/3 need treatment, and as more therapies as they are excisional, which theoretically are better, however, they may compromise the reproductive future of women who are unthreatened, increasing the risk of preterm labor, premature rupture of amniotic membranes, low weight Birth and perinatal mortality. This relationship aroused interest in seeking alternative therapies. Decrease antiviral activity directed against HPV, associated with a higher rate of elimination of the infection. Immediate, an agent that stimulates like dendritic cells to producer cytokines and activates epithelial T cells. Imiquimode, when used in vulvar neoplasias, has been shown to be effective, presenting satisfactory results without treatment of CIN 2/3 of the uterine cervix, requiring a better scientific compilation. Based on these data, this study aims to evaluate the efficacy of topical immunomodulatory treatment for high-grade cervical intraepithelial lesions.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesBrazil
CollaboratorsFarmoquimica S.A.

Timeline

Phase 2CompletedFinished
201820192020202120222023202420252026
First PostedJul 28, 2017
Enrollment StartJan 1, 2018
Primary CompletionJan 14, 2020
TodayJul 2, 2026
Enrollment to primary: 2.0 yearsPosted 8.9 years ago

Interventions

Controlprocedure

Exertion of the cervix transformation zone

Imiquimoddrug

Application by the doctor of immunomodulatory cream on the uterine cervix 1 time per week for 12 weeks