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<title>2019</title>
<link>http://localhost:8080/xmlui/handle/123456789/8046</link>
<description/>
<pubDate>Fri, 10 Apr 2026 21:17:51 GMT</pubDate>
<dc:date>2026-04-10T21:17:51Z</dc:date>
<item>
<title>SYSTEMATIC REVIEW OF YOGASANA AND PRANAYAM IN GARBHINI AND ITS EFFECTS ON PREGNANCY AND BIRTH OUTCOMES</title>
<link>http://localhost:8080/xmlui/handle/123456789/8053</link>
<description>SYSTEMATIC REVIEW OF YOGASANA AND PRANAYAM IN GARBHINI AND ITS EFFECTS ON PREGNANCY AND BIRTH OUTCOMES
KAKLIJ, VIVEK P.
INTRODUCTION: Yoga is an ancient mind-body unifier practice that originated in India. Pregnancy is a condition in which women undergo distinct physiological changes and stress and is accompanied by unique physical and psychological demands. There is a need to manage the various physical, emotional, mental, and pain states that arise throughout the stages of pregnancy and labour. OBJECTIVES:-To do a clinical study on Yogasanas and Pranayama useful in 2nd&amp; 3rd trimester of Pregnancy. DESIGN &amp; SETTING: Comparative clinical study where 30 pregnant women after completion of 16- 18 weeks of gestation were taken from OPD of PTSR department of PIA Hospital and PSH Limda. Two groups of minimum 15 patients each were randomly allocated. Group A (In Trial group): Pregnant women were taught certain Yogasana and Pranayama along with their routine antenatal care then made to practice them everyday throughout antenatal period. In Group B: Pregnant women were advised to follow their routine activities with 30 min walking exercise till the onset of labour. METHODS: The pregnant women responses were assessed on the basis of subjective and objective parameters during antenatal period and Labour. Subjective parameters: During Antenatal Period: Backache, Leg Cramps, Dyspnoea, Fatigability, Sleep and Anxiety. During Labour response to pain coping with contractions at full dilatation of cervix were assessed by following parameters - Bearing down efforts, breathing during labour. Objective parameters: During Antenatal period-Duration of gestation, Biophysical profile scoring, Fixation of head, Engagement of head, Duration of 1st, 2nd &amp; 3rd stage of labour, Quantity of Drug required during labour –Inj. Oxytocin, Inj. Tramadol, birth weight, Apgar score. Study Duration: Minimum 5 months RESULTS AND CONCLUSION: Results were calculated and statistically analyzed using paired and un-paired t-test. The test show significant difference between the two groups. Group A administered Yogasanasa and Pranayama have better effects on Pregnancy, Foetus, labour and Neonate when assessed all the subjective and objective criteria on Group B.
For Full Thesis Kindly contact to respective Library
</description>
<pubDate>Mon, 01 Apr 2019 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://localhost:8080/xmlui/handle/123456789/8053</guid>
<dc:date>2019-04-01T00:00:00Z</dc:date>
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<item>
<title>A COMPARATIVE CLINICAL STUDY OF DHANVANTARA GUTIKA AND BALADI MOOLA GHANAVATI IN GARBHINI UDARSHOOLA IN SECOND TRIMESTER</title>
<link>http://localhost:8080/xmlui/handle/123456789/8050</link>
<description>A COMPARATIVE CLINICAL STUDY OF DHANVANTARA GUTIKA AND BALADI MOOLA GHANAVATI IN GARBHINI UDARSHOOLA IN SECOND TRIMESTER
GHADI, POORNIMA PRAMOD
Introduction: Udarshoola during sagarbhavastha with a variety of causes and presentation can be experienced by women as the body undergoes various physical and physiological changes to accommodate the growing fetus. Udarshoola can be managed by controlling the Vata which is mainly causing the Shoola. Aim &amp; Objectives:Aim-To study the effect of Dhanvantara Gutika and Baladi Moola Ghanavati in Garbhini Udarshoola. Objectives: To have a thorough study on Garbhini Udarshoola and vague abdominal pain in second trimester and to compare the efficacy of the two drugs. Materials &amp; Methods: The study was a single blind randomized comparative clinical study with pre and post test design. Total 30 patients diagnosed with Garbhini Udarshoola and fulfilling the inclusion and exclusion criteria were registered and randomly allocated into two groups. Group A was subjected to Dhanvantara gutika(500 mg) with Ushnodak and Group B was given Baladi Moola Ghanavati with Dugdha and sharkara. Both medicines were administered in vyanodaan kala for 7 days. Dhanvantara Gutika was procured from Vaidyaratnam Pharmacy and Baladi Moola Ghanavati was prepared in the GMP certified pharmaceutical unit of PIA, Vadodara. Assessment was done on Day 2,4 and 7 of treatment for subjective and objective parameters. Results: Results were decided after statistical analysis using Students paired and unpaired ‘t’ test. In group A- 9 Patients and group B- 10 Patients got complete relief. Discussion: Garbhini Udarshoola presented as a Swatantra as well as a Paratantra vyadhi. Dhanvantara Gutika contains Ushna virya dravya which mainly work by their deepana, pachana, shoolahara and anulomana karya. Baladi Moola Ghanavati does Vatashaman by Madhura rasa, Snigdha guna, deepana, pachana and anulomana. Conclusion: Baladi moola ghanavati proved to be more effective than Dhanvantara gutika in curing Garbhini Udarshoola.
For Full Thesis Kindly contact to respective Library
</description>
<pubDate>Tue, 30 Apr 2019 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://localhost:8080/xmlui/handle/123456789/8050</guid>
<dc:date>2019-04-30T00:00:00Z</dc:date>
</item>
<item>
<title>A COMPARATIVE CLINICAL STUDY OF PCOSBLESS AND OVABLESSMYO IN THE MANAGEMENT OF GRANTHIBHUTA ARTAVA DUSHTI W.S.R. TO POLYCYSTIC OVARIAN SYNDROME</title>
<link>http://localhost:8080/xmlui/handle/123456789/8049</link>
<description>A COMPARATIVE CLINICAL STUDY OF PCOSBLESS AND OVABLESSMYO IN THE MANAGEMENT OF GRANTHIBHUTA ARTAVA DUSHTI W.S.R. TO POLYCYSTIC OVARIAN SYNDROME
Parmar, Neha
Introduction- Polycystic ovarian syndrome is the most common endocrinological disorder among women of reproductive age. Based on this the symptomatolgy and causative factors PCOS can be co -related with “granthibhuta artava dushti.” The present study included comparison between trial group of Tablet Pcosbless (anubhuta yoga) and control group of the standard drug Tablet Ovabless-myo for the management of PCOS. Methodology- This study was Open random comparative control clinical trial. The ingredients of Tab Pcosbless were collected in extract form and tablet was prepared at Vasu Pharmacy, Vadodara. Drug Standardization &amp; authentication, preclinical drug safety testing was done before the clinical trial. Out of 30 subjects, 15 were considered under trial group and 15 under control group. The treatment commenced from 5th day of menses and continued for two consecutive menstrual cycles. The response to the treatment was recorded and therapeutic effects were evaluated by symptomatic relief and through USG and Follicular study and LH, FSH, Oestradiol hormone levels. Aims- To study the etiopathogenesis of PCOS by Ayurvedic and modern view. To formulate Simple (Tab Pcosbless) Economical, and palatable tablet for PCOS. Objective:To evaluate the efficacy of Tab Pcossbless on menstrual irregularities &amp; anovulation and to compare its efficacy with the standard drug Tab Ovabless-Myo in PCOS. Result- Total thirty three patients were enrolled in study. Three dropped out of the study, but all remaining thirty patients experienced improvement at the end of treatment. Out of 15 patients completed the treatment in group A, which maximum i.e. 46.7% patients reported marked improved, 33.3% moderate improved and 20% patients mild improved, none of the patients reported unchanged. In group B out of 15 patients completed the treatment, which maximum i.e. 53.3% patients reported marked improved, 46.7% patients Moderate improved, none of the patients reported unchanged. In both groups significant improvement (P&lt;0.005) was observed in symptomatology, but control group was showed higher significant result in ovulation induction. Conclusion- Tab Pcosbless is effective in regularizing menstruation cycle, reducing the ovarian volume and effective in substantial growth of follicles and thus ovulation. Through these achievements Tab Pcosbless has significant improvement in PCOS and will be also effective in cases of infertility caused by PCOS.
For Full Thesis Kindly contact to respective Library
</description>
<pubDate>Mon, 01 Apr 2019 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://localhost:8080/xmlui/handle/123456789/8049</guid>
<dc:date>2019-04-01T00:00:00Z</dc:date>
</item>
<item>
<title>A CLINICAL STUDY TO EVALUATE THE EFFICACY OF SUBIDHABALA KHAND IN GARBHINI CHARDI W.S.R. TO EMESIS GRAVIDARUM</title>
<link>http://localhost:8080/xmlui/handle/123456789/8048</link>
<description>A CLINICAL STUDY TO EVALUATE THE EFFICACY OF SUBIDHABALA KHAND IN GARBHINI CHARDI W.S.R. TO EMESIS GRAVIDARUM
Devi, Mansa
Introduction- Vomiting in pregnancy is the first and foremost symptom of pregnancy. Emesis Gravidarum is a worldwide common obstetrical problem seen in the first trimester of pregnancy in about 50-60 % of pregnant women. Ayurvedic classics have mentioned Garbhini Chardi as one among the Vyakta Garbha Lakshanas, which can be correlated with Emesis Gravidarum. The present study drug Subidhabala khand is used for the management of Garbhini chardi. Methodology- This study was single group clinical trial. The ingredients of Subidhabala khand were collected in the form of raw material and Subidhabala khand (granules) was prepared at Parul Institute of Ayurveda pharmacy, Vadodara. Drug Standardization and authentication, preclinical drug safety testing was done before the clinical trial. The study is a single group clinical study with pre test and post test design was conducted on 30 pregnant women. These patients were selected based on the criteria of inclusion, exclusion and assessment were done as per the standard parameters. 30 patients were given Subidhabala khanda orally in a dose of 6 gm BD before food with Ksheera as Anupana. The response to the treatment was recorded and therapeutic effects were evaluated by symptomatic relief and based on assessment criteria. Aim: To study the Garbhini Chhardi and Emesis Gravidarum in detail. Objective: To assess the effect of Subidhabala khand in Garbhini Chhardi. Result - Total thirty two patients were enrolled in study. Two patients dropped out of the study, but all remaining thirty patients experienced improvement at the end of treatment. In the study significant improvement (P&lt;0.005) was observed in symptomatologically. Conclusion- In the present study, Subidhabala khanda was having good effect in reducing Chardi vegas-44.56%, Hrullas-37.37%, Aruchi-36.07%, Quantity of Vomitus-47.72% and in Content of vomitus-47.72% relief is found and having no any side effect in the health of Garbhini .
For Full Thesis Kindly contact to respective Library
</description>
<pubDate>Mon, 01 Apr 2019 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://localhost:8080/xmlui/handle/123456789/8048</guid>
<dc:date>2019-04-01T00:00:00Z</dc:date>
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