跳至主要内容
临床试验/CTRI/2020/04/024500
CTRI/2020/04/024500尚未招募2 期

Efficacy of Sufoof-i-Tabkheer and Arq-i-Badiyan in Dyspepsia- An open labelled single Arm Clinical Study

ational Institute of Unani Medicine0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Symptoms persist at least for 1 month with moderate to severe symptoms (score > 4 on the 7 point Global overall symptoms (GOS) scale).

排除标准

  • 1.Patients age below 18 and above 50 year
  • 2.Patients with severe systemic and metabolic diseases
  • 3.History of angina pectoris
  • 4.Pregnant and lactating women
  • 5.Patients with alarming symptoms (unintentional weight loss, recurrent vomiting, dysphasia, hematemesis, Malena, fever, jaundice, anemia.
  • 6.History of any serious gastrointestinal disease including peptic ulcer, malignancy, dysmotility.
  • 7.Previous endoscopic diagnosis of erosive gastro-esophagitis or Barrett esophagus.
  • 8.Gastrointestinal surgery within 30 days.
  • 9.Hemoglobin <9g/dl, Total leukocyte count <3000/ul, Platelet count <75000/ul, AST & ALT >120 IU/L, Serum creatinine >1.5 mg/dl, Occult blood in stool.
  • 10.Treatment history of NSAIDs, H2 receptors blockers, PPI, Prokinetic drugs, sucralfate or other ulcer healing agents within 15 days prior to enrolment.
  • 11.Concomitant use of psychotropic drugs.
  • 12.History of alcohol consumption

研究者

发起方
ational Institute of Unani Medicine

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