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Phase

Phase 2 1

Status

Completed 1

Sponsor Class

OTHER 1NETWORK 1

Study Type

Interventional 1

Sponsor

Cancer Type

Gynecologic 1

Conditions

Warts 1Uterine Cervical Neoplasms 1Urinary Tract Infections 1Staphylococcal Infections 1Squamous Intraepithelial Lesions 1Spasm 1Sleep Initiation and Maintenance Disorders 1Sepsis 1Seizures 1Schizophrenia, Treatment-Resistant 1Schizophrenia 1Retinitis 1Renal Insufficiency, Chronic 1Pulmonary Arterial Hypertension 1Pneumonia 1Pain 1Neutropenia 1Migraine Disorders 1Menorrhagia 1Meningitis, Bacterial 1Meningitis 1Intraabdominal Infections 1Influenza, Human 1Inflammation 1Infections 1Hypokalemia 1Hypertension 1Hyperaldosteronism 1High-grade Anal Intraepithelial Neoplasia 1Herpes Simplex 1

Interventions

DNA Methylation 2Colposcopy 2Aminolevulinic Acid 2calcipotriene 1Solutions 1Red Light 1Probiotics 1Observation 1Mindfulness-Based Stress Reduction 1Mass Screening 1Laser Therapy 1Immunohistochemistry 1Gels 1Folic Acid 1Data Collection 1Cidofovir 1Blue Light 1Biopsy 1

Date Range

30 days90 days1 yearAll

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Clinical Trials

1 trials
RecentStart dateEnrollment
OTHER × Squamous Intraepithelial Lesions × Cidofovir × Clear all
NCT02976987 2016-11-30

A Prolongation of a Clinical Study to Evaluate the Efficacy of an Aqueous Gel Containing 2% (w/w) of Cidofovir, Directly Applied on the Cervix Exhibiting High Grade Squamous Intraepithelial Lesions.

Brugmann University Hospital

Phase 2 Completed
36 enrolled
Gynecologic

Squamous Intraepithelial Lesions

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