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Elimination of high-risk human papillomavirus type HPV16 infection by Praneem polyherbal tablet in women with early cervical intraepithelial lesions
Journal of Cancer Research & Clinical Oncology, 06/17/09
Shukla S et al. - In a trial to evaluate potential anti-HPV activity of Praneem in women infected with high-risk HPV type 16 (HPV16), it was reported that a 30-day intra-vaginal application of the Praneem can result in elimination of HPV infection from the uterine cervix.
Methods- 20 women molecularly diagnosed positive for HPV16 infection without or with low grade squamous intraepithelial lesion (LSIL) or inflammation were assigned to receive intra-vaginal, topical application of either Praneem tablet or placebo for 30 days excluding the days of menstrual period.
- They were evaluated for persistence of HPV infection using HPV L1 consensus and HPV16-specific PCR as primary outcome.
- 1 course of Praneem treatment resulted in elimination of HPV in 6 of 10 (60%) cases.
- A repeat treatment of 4 pts with persisting HPV infection resulted in clearance of HPV in 2 additional cases resulting in an overall 80% clearance of HPV16 as against a spontaneous clearance of 10% (1/10) in the placebo arm.
- Elimination of HPV DNA was found to be accompanied by marked improvement in clinical symptoms and cytological abnormalities of Praneem-treated pts.
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