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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06285357
Other study ID # EPISTOP_22
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 19, 2024
Est. completion date December 2025

Study information

Verified date March 2024
Source Lo.Li.Pharma s.r.l
Contact Giovanni Grandi
Phone +390594222830
Email giovanni.grandi@unimore.it
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to test the effect of the administration of a dietary supplement consisting of epigallocatechin gallate (EGCG), vitamin B12 and folic acid in the treatment of infections with papilloma virus of the cervix.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 2025
Est. primary completion date February 2025
Accepts healthy volunteers No
Gender Female
Age group 25 Years to 65 Years
Eligibility Inclusion Criteria: - HR-HPV DNA test positivity Exclusion Criteria: - No HSIL

Study Design


Intervention

Dietary Supplement:
EGCG + folic acid + B12
EGCG + folic acid + B12

Locations

Country Name City State
Italy Azienda Ospedaliero-Universitaria di Modena Modena

Sponsors (1)

Lead Sponsor Collaborator
Lo.Li.Pharma s.r.l

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary HPV DNA test negativity Percentage 8 months of treatment
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