跳至主要内容
临床试验/CTRI/2015/02/005559
CTRI/2015/02/005559招募中未知

THERAPUTIC EVALUATION OF HARIJIVAN OIL FOR PAIN RELIEF

AYUSH ARIHANT INDUSTRIES0 个研究点目标入组 50 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
招募中
入组人数
50

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

  • EITHER SEX AGED BETWEEN 30 TO 65 YEARS
  • PATIENTS WITH PRIMARY BACK, KNEE AND ANY MUSCULAR PAIN
  • WILLING AND ABLE TO PARTICIPATE IN THE STUDY

排除标准

  • HISTORY OF ANY TRAUMA/ FRACTURED JOINT / SURGICAL/DIAGNOSTIC INTERVENTION WITH REFERENCE TO THE AFFECTED JOINT(S).
  • 2.GROSS DISABILITY IN PERFORMING DAILY NORMAL ROUTINE I.E. BED RIDDEN PATIENTS OR CONFINED TO A WHEELCHAIR.
  • 3.PATIENTS WITH CO MORBIDITIES SUCH AS GOUTY ARTHRITIS, RHEUMATOID ARTHRITIS AND PSORIATIC ARTHRITIS.
  • 4.PATIENTS HAVING ANY DEFORMITY OF KNEE HIP OR BACK ALTERING THE GAIT AND POSTURE OF THE PATIENT.
  • 5.PATIENTS WITH UNCONTROLLED HYPERTENSION ( >160/100 MM OF HG).
  • 6.PATIENTS WITH UNCONTROLLED DIABETES MELLITUS{HBA1C >9%}
  • 7.PATIENTS WITH EVIDENCE OF MALIGNANCY.
  • 8.PATIENTS ON PROLONGED ( > 6 WEEKS) MEDICATION WITH CORTICOSTEROIDS, ANTIDEPRESSANTS, ANTICHOLINERGICS, ETC. OR ANY OTHER DRUGS THAT MAY HAVE AN INFLUENCE ON THE OUTCOME OF THE STUDY.
  • 9.PATIENTS WHO HAVE A PAST HISTORY OF ATRIAL FIBRILLATION, ACUTE CORONARY SYNDROME, MYOCARDIAL INFARCTION, STROKE OR SEVERE ARRHYTHMIA IN THE LAST 6 MONTHS.
  • 10.PATIENTS WITH ANY SEVERE RENAL OR HEPATIC OR ANY OTHER DISORDER WHICH MAY INTERFERE IN THE STUDY.
  • 11.PREGNANT / LACTATING WOMAN.
  • 12.PATIENTS WHO ARE CURRENTLY PARTICIPATING IN ANY OTHER CLINICAL TRIAL.
  • 13.ANY OTHER CONDITION WHICH THE PRINCIPAL INVESTIGATOR THINKS MAY JEOPARDIZE THE STUDY.

研究者

相似试验