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Clinical Trials/NCT02016027
NCT02016027UnknownPhase 1

Pharmacological Effect of Carica Folia Mother Tincture in Healthy Individual's Blood Parameter.

Fr Muller Homoeopathic Medical College0 sites60 target enrollmentStarted: September 2013Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 1
Sponsor
Enrollment
60
Primary Endpoint
Increase in platelet count

Study Overview

Brief Summary

AIMS & OBJECTIVES To evaluate the effectiveness of administering of Carica folia mother tincture to healthy individual's Platelet count.

Sample Details:- Students, Doctors and non-teaching staffs of Father Muller Homoeopathic Medical College are taken up for the study. A minimum of 60 persons will be selected and will be divided into two groups, Control & Experiment by lottery method.

Voluntary participation in the study is expected. 30 persons in each group. One group will receive Carica folia mother tincture and other group will receive placebo.

Complete Blood count including platelet count will be measured for all 60 subjects before commencing the study.

The drug namely Carica Folia mother tincture will be procured from Father Muller Homoeopathic Pharmaceutical Division which compiles with the standards of Homoeopathic Pharmacopeia of India.

Daily dosage -30 drops of Carica Folia mother tincture in 30 ml of distilled water morning and night for 3days.

On 4th day complete blood count including platelet count will be estimated for all 60 subjects.

Research Methodology and Statistics:

Pre &Post with Control Design is done. Data from the sample is collected and is subjected to Paired 't' test and unpaired 't' test.

HYPOTHESIS:-

Null hypothesis:

No significant changes in complete blood count and platelet count before and after the intervention.

Alternate hypothesis:

There is significant variation in complete blood count and platelet count before and the intervention.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 25 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • healthy individuals
  • Age group- 18yrs to 25yrs
  • both sexes
  • free from any type of medicinal agent at least 15 days before commence the intervention.

Exclusion Criteria

  • person suffering from any illnesses
  • age group below 18yrs and above 25yrs.
  • person taking any medicinal agents, vitamins or any kinds of supplements will not be considered as subject.

Arms & Interventions

Carica folia Arm

Experimental

Intervention: Carica folia (Drug)

Outcomes

Primary Outcomes

Increase in platelet count

Time Frame: 3 days

Secondary Outcomes

  • Increase in Red Blood Cell count(3 days)

Investigators

Sponsor
Fr Muller Homoeopathic Medical College
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dr Nimai Chandra Dhole

Principal Investigator

Fr Muller Homoeopathic Medical College

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