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Search / Trial NCT06752083

Efficacy of Lentinula Edodes-Derived Supplement (AHCC®) in Promoting Negativity of Persistent HPV Infection

Launched by LIAQUAT UNIVERSITY OF MEDICAL & HEALTH SCIENCES · Dec 27, 2024

Trial Information

Current as of October 26, 2025

Completed

Keywords

ClinConnect Summary

The study investigates the ability of AHCC® (Active Hexose Correlated Compound) to support immune modulation and promote negativity of persistent HPV infections, which are associated with an increased risk of cervical cancer. Participants are categorized into three groups based on vaccination and supplement use. Outcomes include the proportion of participants achieving HPV negativity and the safety and tolerability of the supplement over a 4-6 month period. The study aims to evaluate the potential of AHCC® as a complementary approach for managing persistent HPV infection.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Female participants aged 18 years or older.
  • Persistent HPV infection for at least 6 continuous months, confirmed by DNA-HPV testing.
  • No prior treatment for cervical lesions via conization.
  • No prior HPV vaccination
  • Exclusion Criteria:
  • Current or planned pregnancy during the study period.
  • Immunocompromised status, including known HIV infection.
  • Severe or high-grade cervical lesions.
  • Known allergy or hypersensitivity to AHCC® or vaccine components.

About Liaquat University Of Medical & Health Sciences

Liaquat University of Medical & Health Sciences (LUMHS) is a leading institution dedicated to advancing healthcare through innovative research and clinical trials. With a commitment to improving patient outcomes, LUMHS integrates cutting-edge medical education, comprehensive healthcare services, and rigorous scientific inquiry. The university fosters a collaborative environment for researchers and healthcare professionals, aiming to translate scientific discoveries into practical applications. LUMHS is dedicated to upholding the highest ethical standards in clinical research, ensuring participant safety, and contributing to the global body of medical knowledge.

Locations

Varese, Italy

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported