Clinical Study To Evaluate The Effect Of Pradar Nashak Yoga In Pittaja Asrugdar (AUB-O).

Abnormal uterine bleeding (AUB) is a common condition that affects 10–30% of women of reproductive age group. Up to one-third of women experience AUB in their lifetime.AUB can cause significant morbidity and negatively impact a woman’s physical, social, emotional, and material quality of life. Hence It is time to investigate and construct a clinically and scientifically abnormal uterine bleeding management strategy that is not only cost effective. Chronic AUB can lead to severe Anemia, Infertility & Endometrial cancer. hence, it is need of the hour to treat this disease in time, so that these complications can be avoided and women can lead a healthy life. In modern medicine Hemostatic, Analgesic and Hormonal therapies are advised for abnormal uterine bleeding. Their side effects have led to hormonal imbalances hence it is need of time to have an integrated and comprehensive therapeutic intervention in Ayurveda to prevent recurrence & would overcome thelimitations of modern medicine.

In this study we choose Pradar nashak yoga which contains Yastimadhu Haritaki Amalaki Vibhitaki Lodhr Motha,and Sphatik Madhu as Anupaana which stop the bleeding per vagina . In Ayurvedic classics drugs and formulations which have property of Kashaya and Tikta rasa Sheeta veerya Katu Vipaka Shothahara Grahi Garbhashaya Balya Rakta shodhaka Rakta-stambhana and Vatanulomana properties are described for the treatment of Asrugdar.

A clinical study will be conducted to see the efficacy of Pradar Nashak Yoga in pittaja asrugdar (AUB-O).At first, all participants will be screened to check their eligibility for the study. A total of 30 clinically diagnosed patients will be enrolled in this study after taking informed written consent. After that, the first assessment will be done before drug administration with a validated questionnaire and grading will be done according to the signs and symptoms of the patients. Then the drug therapy will be started and the total duration will be 60 days.Two follow ups will be done each after 30 days. The last assessment will be done on the 60th day and the grading will be given again to see the changes in the signs and symptoms of pittja asrugdar.Signatures on informed consent and patient information sheets will be taken on hard copy, and all other relevant data for the study will be collected. After the collection of all the relevant data, the analysis of the data will be done.