Condition: Human Papillomavirus Infection · Cervical Intraepithelial Neoplasia (CIN) · Low-Grade Squamous Intraepithelial Lesions · Sponsor: Dr. Lutfi Kirdar Kartal Training and Research Hospital
Persistent high-risk human papillomavirus infection is an important precursor of cervical cancer and related cervical lesions. This single-center, randomized, assessor-blinded, parallel-group controlled trial evaluates whether dual-modality immunotherapy consisting of an oral immunomodulator plus a vaginal ovule improves HPV clearance compared with standard supportive care. A total of 76 participants will be randomized in a 1:1 ratio. The primary outcome is HPV clearance confirmed by repeat HPV testing and cervical cytology after the 3-month treatment period. Treatment adherence and adverse events will also be monitored.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
| University of Health Sciences Turkey, Kartal Dr. Lütfi Kırdar City Hospital | Istanbul, Istanbul, Turkey (Türkiye) | — |
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