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临床试验/CTRI/2013/05/003705
CTRI/2013/05/003705已完成2 期

A comparative clinico-experimental evaluation of Rasayana Drugs administered orally & by Basti in the management of Madhumeha w. s. r. to Type-II Diabetes Mellitus

Institute for post graduate teaching and research in Ayurveda Gujarat Ayurved University Jamnagar1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2012年6月26日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
100
试验地点
1
主要终点
blood sugar reduction and reduction in sign and symptoms of diabetes mellitus type 2

研究概览

简要总结

In present clinical trial patient fulfilling inclusioncriteria wererandomly divided into three groups viz; group A in which Madanaphala TailaAnuvasana 160 ml  followed by threeRasayana Basti each of 9 Prasruta (850ml) & one Anuvasana on last day; in aschedule of 21 days was given; second group B inwhich Rasayana Kashaya in adose of 100ml daily in two divided doses beforemeal for 21 days was given & in group C placebo capsule of500 mg twice a day for 21 days was given. Total 91 (91%)patients, i.e. 30 in group A, 30 in group B and 30 in group C completed thecourse of the therapy. Rasayana Basti hasshown 54.55% decrease in polyurea, 50% in turbidity of urine, 53.49% inpolyphagia, 60.87% in polydypsia, 90.91% in leg cramps, 69.57% in burningsensation, 68.75% in numbness, 58.54% in excess sweating, 75% in dryness ofmouth, 65.52% in the weakness, 67.57% in fatigue, 1.72% in the weight loss& 55.56% in the loss of libido. Rasayana Kashaya has shown 54.90% decreasein polyurea, 50% in turbidity of urine, 52.38% in polyphagia, 60% inpolydypsia, 72.22% in leg cramps, 57.58% in burning sensation, 55.56% innumbness, 50% in excess sweating, 100% in dryness of mouth, 58% in theweakness, 65.52% in fatigue, 1.02% in the weight loss & 50% in the loss oflibido. Placebo failed to give any relief however the symptoms aggravated bythe placebo treatment. In patients treated with Rasayana Basti there was adecrease of 5.4% & 6.36% in FBS & PPBS respectively. These changes werestatistically insignificant (p>0.05). In group B there was a statisticallysignificant (p<0.05 & p<0.01 respectively) decrease of 13.02% &21.60% in FBS & PPBS respectively. In group C there was a statisticallyinsignificant (p>0.05) increase of 8.22% in FBS. However, in PPBS 20.62%increase was seen which was statistically significant (p<0.01).  Results suggest that Rasayana Kashaya is superior in glycemic control as compared to RasayanaBasti. However clinical manifestations of Madhumeha are well managed with both Rasayana Basti & Kashaya

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Open Label

入排标准

年龄范围
20.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • •Patient of NIDDM with blood sugar level, FBS- 126 to 220 mg/dl or PPBS- 180 to 300 mg/dl.

排除标准

  • •Patients having age less than 20 years & above 60 years.
  • •Patients of Type-I Diabetes or the patients of Type-II Diabetes taking Insulin.
  • •Patients having complications of Diabetes like Nephropathy, Retinopathy, Diabetic Foot, Carbuncles etc.
  • •Patients having Diabetes in association with other endocrinopathies like Phaeochromocytoma, Acromegaly, Cushing’s syndrome, hyperthyroidism etc.
  • •Patients having drug or chemical induced Type II Diabetes, like glucocorticoids induced or thyroid hormone induced etc.
  • •Patients with genetic syndromes associated with Type II Diabetes like Down’s Syndrome, Klinefelter’s Syndrome, Turner’s Syndrome etc.
  • •Patients complicated with any Cardiovascular diseases, Renal diseases, Carcinoma or any other disease effecting multiple body systems and pregnant women etc.
  • •Patients contraindicated for Bastikarma as per classics.

结局指标

主要结局

blood sugar reduction and reduction in sign and symptoms of diabetes mellitus type 2

时间窗: 21 days

次要结局

  • reduction in sign and symptoms of Madhumeha(21 days)

研究者

发起方
Institute for post graduate teaching and research in Ayurveda Gujarat Ayurved University Jamnagar
申办方类型
Research institution and hospital

研究点 (1)

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