Background: Pregnant women are more prone to vulvovaginitis which is a great challenge for obstetricians today. In , described by , , and both can be compared to vulvovaginitis during pregnancy.
Aims: The present study aimed to evaluate efficacy of in the management of (vulvovaginitis during pregnancy).
Materials And Methods: A total of 80 female patients in the age group of 19-40 years were registered and divided into two groups. In Group A ( = 46), was inserted intravaginally, and in Group B ( = 34), Clingen vaginal suppository was inserted intravaginally once at bed time for 14 days. The effect of therapy was assessed on the basis of relief in subjective and objective criteria, i.e., vaginal smear test.
Results: In subjective parameters, such as , , , and , better result was observed in trial Group A receiving . Highly significant relief ( < 0.001) was observed in fungal infection, and significant relief ( = 0.005) was observed in Gram - negative bacterial infection and pus cells in Group A. In Group A, 34.88% patients had complete remission, marked improvement was found in 34.88% cases, and only 2.32% patients remained unchanged, while in Group B, 33.33% patients reported complete remission, marked improvement was found in 10% cases, and 20% patients remained unchanged.
Conclusion: It was concluded from the clinical trial that is highly effective in reducing subjective and objective variables of and can be introduced as a safe herbal therapy of vaginal discharge during pregnancy.
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http://dx.doi.org/10.4103/ayu.AYU_54_15 | DOI Listing |
Intensive Care Med Exp
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Freie Universität Berlin and Humboldt-Universität Zu Berlin, Department of Anesthesiology and Intensive Care Medicine, Charité-Universitätsmedizin Berlin, Campus Benjamin Franklin, Berlin, Germany.
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Uremic pruritus (UP) is a debilitating condition frequently associated with chronic kidney disease, severely impairing patients' quality of life and contributing to increased mortality. Recent studies have suggested that intravenous sodium thiosulfate (STS) may offer therapeutic relief for pruritus in patients undergoing hemodialysis. To assess its effectiveness, we conducted a systematic review and meta-analysis to explore the potential of intravenous STS in managing UP.
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