| CTRI Number |
CTRI/2026/03/106157 [Registered on: 13/03/2026] Trial Registered Prospectively |
| Last Modified On: |
11/03/2026 |
| Post Graduate Thesis |
Yes |
| Type of Trial |
Interventional |
|
Type of Study
|
Homeopathy |
| Study Design |
Randomized, Parallel Group, Active Controlled Trial |
|
Public Title of Study
|
HOMOEOPATHY IN UROLITHIASIS. |
|
Scientific Title of Study
|
AN INTERVENTIONAL STUDY TO COMPARE THE EFFECTIVENESS BETWEEN
OCIMUM CANUM 3X AND INDIVIDUALIZED HOMOEOPATHIC MEDICINE ON
THE PATIENTS HAVING UROLITHIASIS BASED ON THE ASSESSMENT OF USS
SCORE: AN OPEN-LABEL RANDOMIZED CONTROLLED TRIAL |
| 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 TSERING YANKEY |
| Designation |
POSTGRADUATE SCHOLAR |
| Affiliation |
NATIONAL INSTITUTE OF HOMOEOPATHY |
| Address |
NATIONAL INSTITUTE OF HOMOEOPATHY
OPD NO 124, PRACTICE OF MEDICINE
Sector A-8, Chaudhary Ramdev Chowk, Narela OPD NO 124, PRACTICE OF MEDICINE
Sector A-8, Chaudhary Ramdev Chowk, Narela North West DELHI 110040 India |
| Phone |
9233713143 |
| Fax |
|
| Email |
popopipy2@gmail.com |
|
Details of Contact Person Scientific Query
|
| Name |
DR AJITH KUMAR |
| Designation |
ASSISTANT PROFESSOR, PRACTICE OF MEDICINE |
| Affiliation |
NATIONAL INSTITUTE OF HOMOEOPATHY |
| Address |
OPD NO 124, PRACTICE OF MEDICINE
Sector A-8, Chaudhary Ramdev Chowk, Narela
North West DELHI 110040 India |
| Phone |
9745890190 |
| Fax |
|
| Email |
ajith.nih@gov.in |
|
Details of Contact Person Public Query
|
| Name |
DR TSERING YANKEY |
| Designation |
POSTGRADUATE SCHOLAR |
| Affiliation |
NATIONAL INSTITUTE OF HOMOEOPATHY |
| Address |
NATIONAL INSTITUTE OF HOMOEOPATHY
OPD NO 124, PRACTICE OF MEDICINE
Sector A-8, Chaudhary Ramdev Chowk, Narela OPD NO 124, PRACTICE OF MEDICINE
Sector A-8, Chaudhary Ramdev Chowk, Narela North West DELHI 110040 India |
| Phone |
9233713143 |
| Fax |
|
| Email |
popopipy2@gmail.com |
|
|
Source of Monetary or Material Support
|
|
|
Primary Sponsor
|
| Name |
DR TSERING YANKEY |
| Address |
Sector A-8, Chaudhary Ramdev Chowk, Narela, Delhi-110040. |
| Type of Sponsor |
Other [self] |
|
|
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 TSERING YANKEY |
NATIONAL INSTITUTE OF HOMOEOPATHY |
PRACTICE OF MEDICINE. OPD NO 124, Sector A-8, Chaudhary Ramdev Chowk, Narela, Delhi - 110040 North West DELHI |
9233713143
popopipy2@gmail.com |
|
|
Details of Ethics Committee
|
| No of Ethics Committees= 1 |
| Name of Committee |
Approval Status |
| institutional ethical committee |
Approved |
|
|
Regulatory Clearance Status from DCGI
|
|
|
Health Condition / Problems Studied
|
| Health Type |
Condition |
| Patients |
(1) ICD-10 Condition: N22||Calculus of urinary tract in diseases classified elsewhere, |
|
|
Intervention / Comparator Agent
|
| Type |
Name |
Details |
| Comparator Agent |
individualized homoeopathic medicine |
prescribed according to the totality of symptoms, potency, dose and repetition will be as per homoeopathic principle. all the medicine will be administrated orally for 3 months. |
| Intervention |
Ocimum Canum |
Ocimum Canum 3X/ BD/ 4 globules will be administered for 3 months |
|
|
Inclusion Criteria
|
| Age From |
18.00 Year(s) |
| Age To |
65.00 Year(s) |
| Gender |
Both |
| Details |
a. Patients between the ages of 18 and 65 years.
b. Size of the urinary stone ranging from 3mm to 10 mm.
c. Confirmed diagnosis of renal calculi through ultrasound.
d. Both unilateral and bilateral cases of renal calculi will be considered.
e. Patients willing to adhere to general lifestyle modifications related to diet and fluid
intake during the study period. |
|
| ExclusionCriteria |
| Details |
a. Severe or advanced cases requiring surgical procedures or orthopaedic corrections of
deformities
b. Patients with psychiatric diseases
c. Cases suffering from uncontrolled systemic illness or life-threatening infections or
any other vital organ failure.
d. Cases impacted or with stag horn calculi and cases with severe hydronephrosis as per
ultrasound findings.
e. Gross developmental or structural abnormalities of urinary system (like urethral
stricture)
f. Substance abuse and or dependence
g. Pregnancy, lactation, and women of child bearing potential and not practicing a
reliable method of birth control.
h. Participants undergoing homoeopathic treatment for any other chronic disease for
last 6 months
i. Simultaneous participation in any other clinical trial. |
|
|
Method of Generating Random Sequence
|
Computer generated randomization |
|
Method of Concealment
|
An Open list of random numbers |
|
Blinding/Masking
|
Open Label |
|
Primary Outcome
|
| Outcome |
TimePoints |
To compare the mean change in USS score between Individualized Homoeopathic medicine
(IHM) and Ocimum Cannum 3X in the treatment of urolithiasis at baseline and after 3 months
of intervention. |
assessed at baseline and after 3 months of intervention. |
|
|
Secondary Outcome
|
| Outcome |
TimePoints |
1. MONARCH score will be evaluated to assess the causal attribution between the
interventions and the clinical outcome of the patients after 3 months of intervention
|
assessed at baseline and after 3 months of intervention. |
|
|
Target Sample Size
|
Total Sample Size="44" Sample Size from India="44"
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 3 |
|
Date of First Enrollment (India)
|
25/03/2026 |
| 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="0" Months="6" Days="0" |
|
Recruitment Status of Trial (Global)
|
Not Yet Recruiting |
| 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
|
Urolithiasis is a common and painful condition characterized by the formation of calculi in the urinary tract, including the kidneys, ureters, and bladder. It affects nearly 12% of the global population during their lifetime and is associated with significant morbidity and recurrence. In India, the burden of renal calculi is high, and many patients experience recurrent episodes leading to complications such as renal impairment if not properly managed. Common risk factors include low fluid intake, high dietary salt, high animal protein consumption, and diets rich in oxalates. Clinically, patients frequently present with flank pain, haematuria, dysuria, nausea, and vomiting. Ultrasonography is widely used for the diagnosis and monitoring of urinary calculi as it is non-invasive and easily repeatable.
Homoeopathy has been widely used in the management of urolithiasis, both through individualized constitutional treatment and organ-specific remedies. Individualized Homoeopathic Medicine (IHM) is prescribed based on the totality of symptoms and patient constitution, while Ocimum canum 3X is considered a clinically important remedy for renal colic and urinary calculi, especially right-sided cases with red or sandy urinary sediment. Although both approaches are commonly used in clinical practice, high-quality comparative research evaluating their effectiveness is limited.
The present study is designed as an open-label randomized controlled trial to compare the effectiveness of Individualized Homoeopathic Medicine and Ocimum canum 3X in patients with urolithiasis. A total of 44 patients diagnosed with renal calculi (3–10 mm) through ultrasonography will be recruited from the outpatient department of the National Institute of Homoeopathy, Delhi, and randomly allocated into two groups. Group A will receive individualized homoeopathic medicines based on homoeopathic principles, while Group B will receive Ocimum canum 3X (4 globules twice daily) for a period of three months.
The primary outcome will be assessed using the Urolithiasis Symptom Score (USS), which evaluates the severity of symptoms such as pain/colic, haematuria, dysuria, number of stones, size of stones, and location of stones. Assessments will be conducted at baseline and after three months of intervention. Secondary outcomes will include the MONARCH scale to assess causal attribution of homoeopathic intervention and the ADR probability scale to monitor any adverse drug reactions during the study period.
The findings of this study are expected to provide scientific evidence regarding the comparative effectiveness of individualized homoeopathic treatment and the organ-specific remedy Ocimum canum 3X in the management of urolithiasis, thereby helping clinicians select appropriate homoeopathic treatment strategies for patients with urinary calculi. |