Study of 2LPAPI® on the Clearance of Genital HR-HPV Infections.
Recruiting
Phase 4
Interventional Study
Human Papilloma Virus
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
At a Glance
- Age
- 25 – 45
- Sex
- Female
- Trial phase
- Phase 4
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 284 (estimated)
- Sponsor
- Labo'Life · Industry
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About This Trial
Human papillomavirus (HPV) is a prevalent pathogen, the epidemiology of which has mostly been studied in the uterine cervix and the vagina.
The KCE Report 238Cs (2015) recommends " HR-HPV-positive women should not be offered colposcopy immediately. Triage should be done using cytology for this purpose. If cytological abnormalities (ASCUS+) are found, immediate referral should follow for diagnosis…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Women 25-45 years,
* Women of childbearing age under effective contraception,
* Patient with last cytology less than 3 years and normal or not more than LSIL or CIN I at the histology,
* Patient with current cytology presenting normal, ASC-US, AGUS, LSIL, ASC-H, AGC or LSIL+AS…
Contacts