| CTRI Number |
CTRI/2026/02/103902 [Registered on: 16/02/2026] Trial Registered Prospectively |
| Last Modified On: |
14/02/2026 |
| Post Graduate Thesis |
Yes |
| Type of Trial |
Interventional |
|
Type of Study
|
Ayurveda |
| Study Design |
Randomized, Parallel Group Trial |
|
Public Title of Study
|
To compare the effect of Saptamrita Lauha and Dhatri Lauha in Panduroga |
|
Scientific Title of Study
|
Comparative Clinical Evaluation of Saptamrita Lauha and Dhatri Lauha in Panduroga |
| 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 Pratibha |
| Designation |
Post Graduate Scholar |
| Affiliation |
Patanajali Bhartiya Ayurvigyan Evam Anusandhan Sansthan, Haridwar Delhi Highway,Uttarakhand, India |
| Address |
OPD no. 13,14,Department of Kayachikitsa,Patanajali Bhartiya Ayurvigyan Evam Anusandhan Sansthan, Haridwar Delhi Highway, Uttarakhand, India
Hardwar
UTTARANCHAL
249405
India |
| Phone |
8556869095 |
| Fax |
|
| Email |
pratibhabajaj2@gmail.com |
|
Details of Contact Person
Scientific Query
|
| Name |
Dr Jyoti Arya |
| Designation |
Associate Professor |
| Affiliation |
Patanajali Bhartiya Ayurvigyan Evam Anusandhan Sansthan, Haridwar Delhi Highway, Uttarakhand, India |
| Address |
Patanajali Bhartiya Ayurvigyan Evam Anusandhan Sansthan, Haridwar Delhi Highway, Uttarakhand, India
Hardwar
UTTARANCHAL
249405
India |
| Phone |
9897942660 |
| Fax |
|
| Email |
drjyotiarya@gmail.com |
|
Details of Contact Person
Public Query
|
| Name |
Dr Jyoti Arya |
| Designation |
Associate professor |
| Affiliation |
Patanajali Bhartiya Ayurvigyan Evam Anusandhan Sansthan, Haridwar Delhi Highway,Uttarakhand, India |
| Address |
Patanajali Bhartiya Ayurvigyan Evam Anusandhan Sansthan, Haridwar Delhi Highway, Uttarakhand, India
Hardwar
UTTARANCHAL
249405
India |
| Phone |
9897942660 |
| Fax |
|
| Email |
drjyotiarya@gmail.com |
|
|
Source of Monetary or Material Support
|
| Patanajali Bhartiya Ayurvigyan Evam Anusandhan Sansthan, Haridwar Delhi Highway, Uttarakhand, India |
|
|
Primary Sponsor
|
| Name |
Patanajali Bhartiya Ayurvigyan Evam Anusandhan Sansthan |
| Address |
Patanajali Bhartiya Ayurvigyan Evam Anusandhan Sansthan Haridwar Delhi Highway,Uttarakhand,India 249405 |
| Type of Sponsor |
Private medical college |
|
|
Details of Secondary Sponsor
|
|
|
Countries of Recruitment
|
India |
|
Sites of Study
|
| No of Sites = 1 |
| Name of Principal
Investigator |
Name of Site |
Site Address |
Phone/Fax/Email |
| Dr Pratibha |
Patanjali Bhartiya Ayurvigyan Evam Anusandhan Sansthan |
Department of Kayachikitsa, OPD no.13/14,Patanjali Bhartiya Ayurvigyan Evam Anusandhan Sansthan, Haridwar Delhi Highway, Uttarakhand 249405
Hardwar
UTTARANCHAL |
8556869095
pratibhabajaj2@gmail.com |
|
|
Details of Ethics Committee
|
| No of Ethics Committees= 1 |
| Name of Committee |
Approval Status |
| INSTITUTIONAL ETHICS COMMITTEE, PATANJALI BHARTIYA AYURVIGYAN EVAM ANUSANDHAN SANSTHAN, HARIDWAR |
Approved |
|
|
Regulatory Clearance Status from DCGI
|
|
|
Health Condition / Problems Studied
|
| Health Type |
Condition |
| Patients |
(1) ICD-10 Condition:E611||Iron deficiency. Ayurveda Condition: PANDUROGAH, |
|
|
Intervention / Comparator Agent
|
| sno | Intervention/Comparator | Type | Drug-Type | Procedure Name | Details | | 1 | Intervention Arm | Drug | Classical | | (1) Medicine Name: Saptamrit lauha , Reference: : Bhaishyajya Ratnavali, Route: Oral, Dosage Form: Churna/ Powder, Dose: 500(mg), Frequency: bd, Bhaishajya Kal: Adhobhakta, Duration: 60 Days, anupAna/sahapAna: Yes(details: -Honey ), Additional Information: - | | 2 | Comparator Arm | Drug | Classical | | (1) Medicine Name: Dhatri lauha , Reference: Bhaishyajya Ratnavali, Route: Oral, Dosage Form: Churna/ Powder, Dose: 500(mg), Frequency: bd, Bhaishajya Kal: Adhobhakta, Duration: 60 Days, anupAna/sahapAna: Yes(details: -Honey ), Additional Information: - |
|
|
|
Inclusion Criteria
|
| Age From |
18.00 Year(s) |
| Age To |
60.00 Year(s) |
| Gender |
Both |
| Details |
Male or females having classical symptoms of Panduroga.
Hb levels in males- 10gm%- 13gm% and in females- 8gm%- 11gm%.
Age 18 to 60 years.
Diagnosed patients without any complication.
Willingness to sign the consent form.
|
|
| ExclusionCriteria |
| Details |
Pregnant and lactating women.
Hb levels less than 8gm%.
Malignancy, Kidney Disease, Thalassemia, Cardiac Disorders, Anemia due to any other causes other than Iron Deficiency.
|
|
|
Method of Generating Random Sequence
|
Computer generated randomization |
|
Method of Concealment
|
On-site computer system |
|
Blinding/Masking
|
Open Label |
|
Primary Outcome
|
| Outcome |
TimePoints |
Reduction in -
Panduta (pallor)
Hridayaspandan (palpitation)
Pindikodweshtana (cramps in calf region)
Aayasena shwasa (exertion dyspnoea)
Arochaka (anorexia )
Daurbalya (weakness) |
Day 30, Day 60 |
|
|
Secondary Outcome
|
| Outcome |
TimePoints |
Improvement in
HB levels
MCV
MCH
Reducing RDW |
Day 30, Day 60 |
|
|
Target Sample Size
|
Total Sample Size="60"
Sample Size from India="60"
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
|
Phase 2/ Phase 3 |
|
Date of First Enrollment (India)
|
25/02/2026 |
| 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="6"
Days="0" |
|
Recruitment Status of Trial (Global)
|
Not Applicable |
| Recruitment Status of Trial (India) |
Not Yet Recruiting |
|
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 double arm clinical evaluation of Saptamrita lauha and Dhatri lauha in Panduroga (Iron deficiency anemia).This will be conducted on 60 randomly selected patients from OPD of Kayachikitsa department of Patanjali Ayurved Hospital, Haridwar. First follow up during treatment - 30 days and second follow up at the end of treatment i.e. 60 days. Assessment will be done on basis of subjective and objective parameters as discussed earlier. |