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A Safety and Efficacy of Homeopathic Medicine Rhus Toxicodendron 30 in the Treatment of Rheumatoid Arthritis

H

Healthcare Homoeo Charitable Society

Status and phase

Unknown
Phase 2

Conditions

Rheumatoid Arthritis.

Treatments

Drug: Rhustoxicodendron 30
Drug: placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT01905735
SLSGB-01

Details and patient eligibility

About

the purpose of the study is to assess the safety and efficacy of commonly used Homeopathic medicine Rhustoxicodendron in 30 potency in the treatment of Rheumatoid arthritis.

Full description

it is a multicenter phase 2 ,double blind study in patient with active Rheumatoid arthritis ,there are 2 group in the study A and B ,where group A receive Rhustoxicodendron in 30 potency the first dose will administered orally (1/2 ml)after the completion of case taking ,and repeated every 7th day for 5 month and on the other hand group B receive placebo orally in (1/2 ml) at same interval for same period .

Enrollment

60 estimated patients

Sex

All

Ages

25 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • those who will provide written consent to participate in the study
  • patient willing to turn up for 7th day follow up
  • patient who are willing and compliance to the study
  • those who are between 25 to 60 years .
  • patient who are willing and compliance to the study .
  • ESR more then 28 mm.

Exclusion criteria

  • Participating as a subject in any other clinical research study.
  • Children below the age of 25years.
  • Female subject who are pregnant or planning for pregnancy within 6 month.
  • History of seizures
  • Breast feeding women's.
  • Patient on treatment for life threatening illness like cancer aids etc.
  • Patient should not have any congenital abnormality or patient should not have undergone any operative procedure as consequences of RA.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups, including a placebo group

placebo
Placebo Comparator group
Description:
1/2 ml of dispensing alcohol administered orally at every 7 day for 5 month .
Treatment:
Drug: placebo
Rhustoxicodendron 30
Active Comparator group
Description:
1/2ml Rhustoxicodendron 30 is administered orally every 7 day for 5 month.
Treatment:
Drug: Rhustoxicodendron 30

Trial contacts and locations

2

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Central trial contact

mukesh k singh, B.H.M.S; seenia sharma, B.H.M.S

Data sourced from clinicaltrials.gov

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