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Pharmacological Effect of Carica Papaya Leaves Mother Tincture in Healthy Individuals Blood Parameter

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

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02016027
Acronym
CF2013
Enrollment
60
Registered
2013-12-19
Start date
2013-09-30
Completion date
2013-12-31
Last updated
2013-12-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dengue

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.

Interventions

DRUGCarica folia

Sponsors

Fr Muller Homoeopathic Medical College
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 25 Years
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.

Design outcomes

Primary

MeasureTime frame
Increase in platelet count3 days

Secondary

MeasureTime frame
Increase in Red Blood Cell count3 days

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026