首页> 外文期刊>International Journal of Pharmaceutical Sciences and Research >EFFICACY OF MUNZIJ WA MUSHIL-E-BALGHAM (POLY HERBAL FORMULATIONS) AND MASSAGE WITH ROGHAN-E-MALKANGANI IN FALIJ NISFI (HEMIPLEGIA): A RANDOMISED CONTROLLED CLINICAL TRIAL
【24h】

EFFICACY OF MUNZIJ WA MUSHIL-E-BALGHAM (POLY HERBAL FORMULATIONS) AND MASSAGE WITH ROGHAN-E-MALKANGANI IN FALIJ NISFI (HEMIPLEGIA): A RANDOMISED CONTROLLED CLINICAL TRIAL

机译:Munzij Wa Mushil-e-Balgham(Poly Herbal制剂)和按摩与罗汉-e-Malkangani(偏瘫)(偏瘫)(偏瘫)的疗效:随机对照临床试验

获取原文
           

摘要

This study was conducted as a single blind, randomized and standard controlled clinical trial in cases of Falij Nisfi (Hemiplegia) due to ischaemic stroke. Forty eligible patients of Hemiplegia were randomized into test and control groups, comprising 20 patients in each. Test group was given Nuskha munzije balghamfor12 days, followed byNuskha Mushile Balgham, mixed with Munzije Balgham for next two consecutive days in decoction form, orally. Massage was started from 15th day with Roghan Malkangani on spinal column and paralyzed limbs for 15 minutes daily till 28th day. Control group was given tablet Piracetam Hydrochloride, 800 mg twice a day. Hypertensive patients in both groups, A and B, also received tablet Aspirin, 75 mg and tablet lisinopril, 2.5 mg, once daily for 28 days. The assessment of efficacy was based on “Stroke Rehabilitation Assessment of Movement (STREAM)”. Pre and post treatment values of STREAM were subjected to statistical analysis within and between the groups using Paired‘t’ test, Wilcoxon matched pairs signed rank test, and Kruskal-Wallis test with Dunn’s multiple comparison test. There was significant improvement in STREAM scores for voluntary movements of upper limb (P<0.01), lower limb (P<0.01), Basic mobility (P<0.01), and total score (P<0.01), in test Group as compared to control Group. The study revealed that test drug has statistically significant response in improving voluntary movements as compared to control drug.
机译:该研究是由于缺血性卒中因缺血性脑卒中而在Falijnisfi(偏瘫)病例中进行的单一盲,随机和标准对照临床试验。四十个符合条件的偏瘫患者被随机转变为试验和对照组,每组20名患者。考试组给予Nuskha Munzije Balghamfor 12天,遵循了Bynuskha Mushile Balgham,与Munzije Balgham混合在一起连续两天,口服。按摩从15个 th 日开始,脊柱柱和瘫痪的四肢每天15分钟,直到28 th 日。对照组给予片剂皮卡替昔伐盐酸盐,每天两次800毫克。两组,A和B中的高血压患者,也接受了平板药物,75毫克和片剂乳突素,2.5毫克,每日一次28天。疗效评估是基于“运动康复评估(流)”。使用PERED'TET'TIST'TERINGES,WILCOXON匹配对符号试验和kruskal-wallis试验进行统计分析,在组之间进行统计分析,与DUNN的多个比较试验进行统计的秩序。对于上肢的自愿运动(P <0.01),下肢(P <0.01),基本迁移率(P <0.01)和总分(P <0.01),以及测试组的流量分数存在显着改善控制组。该研究表明,与对照药物相比,测试药物在改善自愿运动方面具有统计学意义。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号