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CTRI Number  CTRI/2026/01/102126 [Registered on: 27/01/2026] Trial Registered Prospectively
Last Modified On: 23/09/2026
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Homeopathy 
Study Design  Non-randomized, Multiple Arm Trial 
Public Title of Study   A comparative study of homoeopathic decimal and centesimal scales in treatment of hair falling in aged 20-50 years using the hair shedding visual scale and hair pull test 
Scientific Title of Study   A comparative study: effectiveness of homoeopathic decimal and centesimal scales in the management of telogen effluvium aged 20–50 years using the HSVS and hair pull test –a individualised approach 
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Poojabahen Kanubhai Parmar 
Designation  PG Scholar 
Affiliation  Parul institute of homoeopathy and research hospital 
Address  Parul institute of homoeopathy and research hospital,3rd floor room no.401, Department of Homoeopathic Pharmacy, At. Ishwarpura po. Limda Ta. Waghodia di. Vadodara

Vadodara
GUJARAT
391760
India 
Phone  9484463452  
Fax    
Email  poojakparmar78@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Nayana Patel 
Designation  Associate Professor 
Affiliation  Parul institute of homoeopathy and research hospital 
Address  Parul institute of homoeopathy and research hospital,3rd floor room no.401, Department of Homoeopathic Pharmacy, At. Ishwarpura po. Limda Ta. Waghodia di. Vadodara

Vadodara
GUJARAT
391760
India 
Phone  8128815189  
Fax    
Email  nayanaben.patel17843@paruluniversity.ac.in  
 
Details of Contact Person
Public Query
 
Name  Poojabahen Kanubhai Parmar 
Designation  PG Scholar 
Affiliation  Parul institute of homoeopathy and research hospital 
Address  Parul institute of homoeopathy and research hospital,3rd floor room no.401, Department of Homoeopathic Pharmacy, At. Ishwarpura po. Limda Ta. Waghodia di. Vadodara

Vadodara
GUJARAT
391760
India 
Phone  9484463452  
Fax    
Email  poojakparmar78@gmail.com  
 
Source of Monetary or Material Support  
Parul Institute of Homoeopathy and Research Hospital 
 
Primary Sponsor  
Name  Parul Institute of Homoeopathy and Research  
Address  Parul Institute of Homoeopathy and Research, At. Ishwarpura, Po. Limda, Ta. Waghodia, Di. Vadodara-391760 
Type of Sponsor  Research institution and hospital 
 
Details of Secondary Sponsor  
Name  Address 
Poojabahen Kanubhai Parmar  Parul Institute of Homoeopathy and Research, At. Ishwarpura, Po. Limda, Ta. Waghodia, Di. Vadodara-391760 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Poojabahen Kanubhai Parmar  Parul Institute of Homoeopathy and Research Hospital  Parul Institute of Homoeopathy and Research Hospital,3rd floor, room no,401, department of Homoeopathic Pharmacy AT. Ishwarpura, po. Limda, ta. Waghodia di. Vadodara
Vadodara
GUJARAT 
9484463452

poojakparmar78@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethical Committee For Human Research  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: L650||Telogen effluvium,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Individualised homoeopathic medicine  The intervention in this study is Participants diagnosed with Telogen Effluvium and fulfilling the inclusion criteria will receive individualised homoeopathic treatment based on the totality of symptoms. Remedies will be selected according to homoeopathic principles and prescribed in either decimal or centesimal potency scales. Participants will be allocated into two groups based on the potency scale used. The prescribed medicines will be administered in appropriate dosage and repetition as per individual case requirement. Follow-up assessments will be conducted every 15 days to evaluate treatment response, adjust potency or medicine if required, and monitor outcomes using the Hair Shedding Visual Scale (HSVS) and Hair Pull Test. The medicine will be administered through the oral route. 
Comparator Agent  Not applicable  Not applicable 
 
Inclusion Criteria  
Age From  20.00 Year(s)
Age To  50.00 Year(s)
Gender  Both 
Details  Patients diagnosed with telogen effluvium, confirmed through clinical history and positive hair pull test.
Post-febrile illness (e.g., after dengue, typhoid, covid-19, influenza). postpartum state (within 12 months of delivery). Psychological stress, anemia, scalp infections or fungal diseases.
 
 
ExclusionCriteria 
Details  Patients with other forms of alopecia (e.g., alopecia areata, androgenetic alopecia, scarring alopecia).
Pregnant or lactating women.
Patients with underlying systemic disorders like: autoimmune diseases (e.g., lupus), diabetes mellitus, pcod, thyroid disorder and also patients on chemotherapy or radiotherapy.
Patients currently using or having recently used topical steroids, minoxidil, or systemic treatments for hair loss.
 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
To evaluate the usefulness of decimal and centesimal scale in the management of telogen effluvium.  3 months 
 
Secondary Outcome  
Outcome  TimePoints 
To assess improvement in hair fall using hair shedding visual scale.  3 months 
 
Target Sample Size   Total Sample Size="30"
Sample Size from India="30" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   N/A 
Date of First Enrollment (India)   02/03/2026 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="1"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
Recruitment Status of Trial (India)  Open to Recruitment 
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 comparative clinical study design to evaluate the usefulness of Homoeopathic medicines prescribed in decimal and centesimal scale in the management of Telogen Effluvium in aged group 20-50 years. The study will be conducted at Parul Institute of Homoeopathy and Research Hospital, Vadodara, with a total sample size of 30 patients and a study duration of 3 months. Each patient will receive  individualised homoeopathic treatment based on detailed case taking and totality of symptoms. the outcome of the study will be the assessment of improvement in hair shedding by using hair shedding visual scale and hair pull test before and after treatment and also in every follow ups. Patients will be divided into two groups, each receiving homoeopathic treatment in either decimal or centesimal potency scales. The results will be statistically analyzed to compare the efficacy of both scales. The study aims to provide scientific evidence regarding the most effective potency scale in the management of telogen effluvium. 
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