Pharmacological Effect of Carica Papaya Leaves Mother Tincture in Healthy Individuals Blood Parameter
NCT ID: NCT02016027
Last Updated: 2013-12-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
PHASE1
60 participants
INTERVENTIONAL
2013-09-30
2013-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Carica folia Arm
Carica folia
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Carica folia
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Age group- 18yrs to 25yrs
* both sexes
* free from any type of medicinal agent at least 15 days before commence the intervention.
Exclusion Criteria
* age group below 18yrs and above 25yrs.
* person taking any medicinal agents, vitamins or any kinds of supplements will not be considered as subject.
18 Years
25 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Fr Muller Homoeopathic Medical College
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Dr Nimai Chandra Dhole
Principal Investigator
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
NCD
Identifier Type: -
Identifier Source: secondary_id
carica 2013
Identifier Type: -
Identifier Source: org_study_id