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SYNOPSIS FOR
PROPOSED THESIS WORK FOR THE DEGREE OF AYURVEDA VACHASPATI
M.D. (Ayu.) DRAVYAGUNA
TITLE
“Identification of different species used as ‘Chukrika’ & To evaluate the clinical
efficacy of Rumex vasicarius Linn. in Arochak”
Research Scholar
Dr. Kailash rana
B.A.M.S. (H.P.U.)
Respected Sir,
Kindly allow me to submit synopsis for registration of title for the degree of Ayurveda
Vachaspati M.D. (Ayu.) Dravyaguna. Please find enclosed herewith synopsis of my thesis work
Thanking you,
Date……………. Yours sincerely,
This is to certify that the plan of the proposed research work entitled “Identification of
different species used as ‘Chukrika’ & To evaluate the clinical efficacy of ‘Rumex
vasicarius Linn. in Arochak” has been prepared by Dr. Kailash rana under our supervision
and further research work will also be carried out during M.D.(Ayu.) course under the guidance
of the undersigned.
Co-Guide
Prof. Ashwani Upadhyaya --------------------------
M.D.(Ayu.) Ph.D.
Head of Deptt.
P. G. Deptt. Of Dravyaguna
R.G.G.P.G. Ayurvedic College and Hospital,
Paprola, Kangra (H.P.) 176115
Supervisor Scholar
“ वृद्ध भोज”
“भा.प्र”
Review of literature
A detailed review of different species of Chukrika will be done from Ayurvedic and
Modern literature, journals and recent research works.
Ayurvedic and modern literature will be reviewed thoroughly to know Arochak in detail
and its treatment, according to Ayurvedic therapeutics.
INTRODUCTION OF DRUG
PLANT DESCRIPTION:
Name of Drug - Chukrika
Botanical Name - Rumex vasicarius Linn.
Family - Polygonaceae
PROPERTIES AND ACTIONS:
Rasa - Amal, Madhur
Guna - Laghu
Veerya - Ushna
Vipaka - Amal
“भा.प्र”
On the basis of this reference this drug has been selected for present research work.
Pharmacognostical study:
Detailed macroscopic and microscopic study on different species used as Chukrika of trial drug
will be done in the department of Dravyaguna.
Preparation of drug:
The selected drug will be collected locally and after proper verification by the experts of Deptt. Of
Dravyaguna, the final drug will be prepared under the guidance of Deptt. of Rasa Shastra evum
Bhaishjya Kalpana in the college pharmacy.
Formulation:
Clinical study:
Clinical study will be done on the patients selected from OPD and IPD of R. G. G. P. G.
Ayurvedic College and Hospital, Paprola, Distt. Kangra(H.P.), irrespective of caste and religion.
Complete description regarding the details of each research case will be recorded in a prepared
proforma.
8. Protocol for clinical study >>
• The ethical clearance will be taken for the research from Institutional Ethics Committee
(IEC) before starting the study.
• Consent of patient: Awareness about the duration and nature of the trial and written
informed consent.
1. Inclusion criteria
8.4. Follow up
There will be a follow up on 5TH and 10TH days during treatment and one after completion of
trial.
Diagnosis criteria- A proforma will be prepared, incorporating all the signs and symptoms
of disease and other related information regarding the problem.
Effect of therapy will be assessed according to improvement in signs and symptom of Arochak.
9.1. INVESTIGATIONS
Laboratory investigations
Estimation of CBC will be carried out for general assessment of patients before and after
trial.
Criteria of assessment is kept on the basis of relief in the sign and symptoms of the disease
Arochak. All the patients will be examined after three days of treatment and completion of trial.
Assessment will be done on the basis of following criteria.
Grading of assessment criteria
o Annaabhilasha
Grade 0 - No Annaabhilasha
Grade 2 - Sometime not willing to eat, but don’t take food regularly
Grade 3 - Not willing to eat all.
Kashaya asayata
o Madhur asayata
Grade 0 - Absent
Patients will be assessed before and after the treatment for improvement in symptoms on the
basis of above said scoring pattern and percentage improvement will be calculated.
Statistical Analysis:
The result thus obtained from individual patient will be categorized according to the
following grades:
Cured - 100% relief in symptoms
REQUIREMENTS
o Well established library.
o Raw drug and other equipments for processing of drug.
This is expected that the findings obtained through this research trial will certainly prove fruitful
to enrich the present knowledge of subject.
Name of Patient -
I have been given the opportunity to question Dr. Kailash Rana on all aspects of the study. I
hope to complete the study but I am also aware of my right to withdraw at any time during the
course of study without any reason.
I have been informed to my satisfaction about the trial and agree to take part in clinical trial
for a period of 15 days.
I will not make any claim for compensation for any hazardous effect if it occurs during or
after the treatment.
I confirm that I have explained the nature, purpose and possible hazards of the above
mentioned study to Mr./Mrs………………………….
Study title - “Identification of different species used as Chukrika & To evaluate the
clinical efficacy of Rumex vasicarius Linn. in Arochak”
Procedure of the trial – If you are agree to take part in this study, you will be given
Chukrika patar Churan two times orally in 5gms dose for period of 15 days.
You have to undergo investigation before and after the trial for assessment.
Expected untowards effects - The trial drug as such involves no untowards effects
but yet individual specific variations may occur at any time during the course of clinical
trial.
If you want to ask anything about the clinical trial, you are free to ask at any stage of
trial. A copy of the information sheet and signed consent form will also be given to you.
All your information will be kept confidential and the result will be published in
leading medical journals so that other doctors get benefit from the result.
Signature Date