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CTRI Number  CTRI/2025/01/079769 [Registered on: 29/01/2025] Trial Registered Prospectively
Last Modified On: 20/11/2025
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Homeopathy 
Study Design  Single Arm Study 
Public Title of Study   Role of murphy repertory in the management of chronic urticaria 
Scientific Title of Study   Utility of homoeopathic medical repertory by Robin murphy in the management of chronic Urticaria assessed by urticaria activity score 
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  DR ARPITABEN RAJNIKANTBHAI PATEL 
Designation  PG SCHOLAR 
Affiliation  SMT A J SAVLA HOMOEOPATHIC MEDICAL COLLEGE AND RESEARCH INSTITUTE 
Address  DEPARTMENT OF MEDICINE ROOM NO 6 GROUND FLOOR SMT A J SAVLA HOMOEOPATHIC MEDICAL COLLEGE AND RESEARCH INSTITUTE PUSHPANJALI BUILDING NEAR DISTRICT SESSION COURT MEHSANA

Mahesana
GUJARAT
384001
India 
Phone  8401766070  
Fax    
Email  arpita53201@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  DR GAURANG CHHAYA 
Designation  PROFESSOR 
Affiliation  SMT A J SAVLA HOMOEOPATHIC MEDICAL COLLEGE AND RESEARCH INSTITUTE 
Address  DEPARTMENT OF HOMOEOPATHIC REPERTORY AND CASE TAKING ROOM NO 14 FIRST FLOOR SMT A J SAVLA HOMOEOPATHIC MEDICAL COLLEGE AND RESEARCH INSTITUTE PUSHPANJALI BUILDING NEAR DISTRICT SESSION COURT MEHSANA

Mahesana
GUJARAT
384001
India 
Phone  9979953933  
Fax    
Email  chhayagaurang62@gmail.com  
 
Details of Contact Person
Public Query
 
Name  DR ARPITABEN RAJNIKANTBHAI PATEL 
Designation  PG SCHOLAR 
Affiliation  SMT A J SAVLA HOMOEOPATHIC MEDICAL COLLEGE AND RESEARCH INSTITUTE 
Address  DEPARTMENT OF MEDICINE ROOM NO 6 GROUND FLOOR SMT A J SAVLA HOMOEOPATHIC MEDICAL COLLEGE AND RESEARCH INSTITUTE PUSHPANJALI BUILDING NEAR DISTRICT SESSION COURT MEHSANA

Mahesana
GUJARAT
384001
India 
Phone  8401766070  
Fax    
Email  arpita53201@gmail.com  
 
Source of Monetary or Material Support  
SMT A J SAVLA HOMOEOPATHIC MEDICAL COLLAGE AND RESEARCH INSTITUTE PUSHPANJALI BUILDING NEAR DISTRICT SESSION COURT MEHSANA GUJARAT 384001 
 
Primary Sponsor  
Name  DR ARPITABEN RAJNIKANTBHAI PATEL 
Address  DEPARTMENT OF MEDICINE ROOM NO 6 GROUND FLOOR SMT A J SAVLA HOMOEOPATHIC MEDICAL COLLEGE AND RESEARCH INSTITUTE PUSHPANJALI BUILDING NEAR DISTRICT SESSION COURT MEHSANA GUJARAT 384001  
Type of Sponsor  Other [SELF] 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
DR ARPITABEN RAJNIKANTBHAI PATEL  SMT A J SAVLA HOMOEOPATHIC MEDICAL COLLEGE AND RESEARCH INSTITUTE  DEPARTMENT OF MEDICINE ROOM NO 6 PUSHPANJALI BUILDING NEAR DISTRICT SESSION COURT MEHSANA GUJARAT 384001
Mahesana
GUJARAT 
8401766070

arpita53201@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
SMT A J SAVLA HOMOEOPATHIC MEDICAL COLLEGE AND RESERCH INSTITUTE INSTITUTIONAL ETHICAL COMMITTEE  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: L508||Other urticaria,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  HOMOEOPATHIC MEDICINE  POTENCY VERIOUS DOSES AS PER NEED OF CASE FREQUENCY AS PER NEED OF CASE ROTE OF ADMINISTRATION ORAL DURATION OF 8 MONTH AS PER NEED OF CASE  
Comparator Agent  NIL  NIL 
 
Inclusion Criteria  
Age From  20.00 Year(s)
Age To  40.00 Year(s)
Gender  Both 
Details  Age group people from 20 to 40 years age group
Gender Male and Female
Case presenting with symptoms of chronic urticaria
Patient will be selected on the basis of clinically diagnosed characteristics of erythema and itchy lesions which is subside within 24 hour
Patients who gave voluntary consent and be able to fill the Urticaria Activity Score to be included in the study
Urticaria Activity Score over 1 week cases range between 7 to 27 include mild and moderate urticaria according Urticaria Activity Score
 
 
ExclusionCriteria 
Details  Pregnant women and lactating women were not included in the study
Patient having other co morbid conditions associated with chronic urticaria such as thyroid disease inflammatory disease DM malignancy
Vasculitic urticaria angioedema with no urticaria anaphylaxia
Patient taking any mode of treatment like allopathic homoeopathic ayurvedic for urticaria
 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Participant Blinded 
Primary Outcome  
Outcome  TimePoints 
URTICARIA ACTIVITY SCORE TO ASSESS REDUCTION IN URTICARIA SYMPTOMS  SCORE WILL BE ASSESSED AT BASELINE AND EVERYMONTH OF TREATMENT AND AS PER REQUIREMENT OF CASES 
 
Secondary Outcome  
Outcome  TimePoints 
NIL  NIL 
 
Target Sample Size   Total Sample Size="40"
Sample Size from India="40" 
Final Enrollment numbers achieved (Total)= "40"
Final Enrollment numbers achieved (India)="40" 
Phase of Trial   Phase 2/ Phase 3 
Date of First Enrollment (India)   10/02/2025 
Date of Study Completion (India) 10/10/2025 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) 10/10/2025 
Estimated Duration of Trial   Years="1"
Months="6"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Completed 
Recruitment Status of Trial (India)  Completed 
Publication Details   N/A 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary  

THIS STUDY IS A PROSPECTIVE STUDY PRE TEST POST TEST ONE GROUP EXPERIMENTAL STUDY TO ASSESS THE UTILITY OF HOMOEOPATHY MEDICAL REPERTORY BY ROBIN MURPHY FOR 8 MONTHS IN 40 PARTICIPANTS WITH CHRONIC URTICARIA THAT WILL BE CONDUCTED AS PER INCLUSION AND EXCLUSION CRITERIA FROM OUT PATIENT DEPARTMENT AND THE OUTCOMES MEASURES WILL BE ASSESS WITH  URTICARIA  ACTIVITY SCORE AT EVERY MONTH UPTO 8 MONTH PARTICIPANTS FOLLOW UP AT EVERY MONTH AND AS PER NEED OF CASE FOR 8 MONTHS OF DURATION

 
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