Clinical Effectiveness of PAPILOCARE® in Regression of Cervix HPV Cytological Abnormalities (PAPILOBS GR).
- Disease/Condition
- Papillomavirus Infections
- Drug/Device/Intervention
- Papilocare vaginal gel
- Study type
- Observational
- Intervention type
- device
- Primary sponsor
- Elpen Pharmaceutical Co. Inc.
- Location
- Ioannina,Larissa,Patra,Thessaloniki, Greece
- Phase
- N/A
- Start date
- Sep 01, 2021
- End date
- Apr 30, 2023
- Enrollment
- 524 participants
The assessment of effectiveness of PAPILOCARE® in the regression of cervix cytological abnormalities caused by HPV.
The present study is a multicenter, open, non-interventional, prospective observational
 clinical study for the evaluation of the effectiveness of Papilocare® (medical device with CE
 mark) in the regression of cervix cytological abnormalities caused by HPV.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06399341
- Type
- Device Trial
Access comprehensive clinical trial information for NCT06399341 through Pure Global AI's free database. This phase not specified trial is sponsored by Elpen Pharmaceutical Co. Inc. and is currently Completed. The study focuses on Papillomavirus Infections. Target enrollment is 524 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.