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CTRI Number  CTRI/2024/06/068735 [Registered on: 11/06/2024] Trial Registered Prospectively
Last Modified On: 01/10/2024
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Drug
Siddha 
Study Design  Single Arm Study 
Public Title of Study   A Study on Mandurathi Kudineer in the management of Kaleeral Noi (Non-Alcoholic Fatty Liver Disease). 
Scientific Title of Study   An Open Clinical Trial to evaluate the effectiveness of Mandurathi Kudineer in the management of Kaleeral Noi (Non-Alcoholic Fatty Liver Disease) among out patients attending Ayothidoss Pandithar Hospital, National Institute Of Siddha. 
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 R S Suma 
Designation  PG Scholar 
Affiliation  National Institute of Siddha 
Address  Room no:7/8, Department of Maruthuvam,National Institute Of Siddha,Tambaram Sanatorium, Chennai.

Kancheepuram
TAMIL NADU
600047
India 
Phone  9994405417  
Fax    
Email  sumasiddha@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr T Lakshmikantham 
Designation  Associate Proffessor and Head of the Department i/c 
Affiliation  National Institute of Siddha 
Address  Room no:7/8,Department of Maruthuvam, National Institute Of Siddha, Tambaram Sanatorium, Chennai.

Kancheepuram
TAMIL NADU
600047
India 
Phone  9025575185  
Fax    
Email  drlakshmiramasway@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr T Lakshmikantham 
Designation  Associate Proffessor And Head of the Department i/c 
Affiliation  National Institute of Siddha 
Address  Room no:7/8 ,Department of Maruthuvam ,National Institute of Siddha,Tambaram Sanatorium, Chennai.

Kancheepuram
TAMIL NADU
600047
India 
Phone  9025575185  
Fax    
Email  drlakshmiramasway@gmail.com  
 
Source of Monetary or Material Support  
National Institute Of Siddha , Tambaram Sanatorium, Chennai-47 
 
Primary Sponsor  
Name  National Institute of Siddha 
Address  Room no:7/8,Department of Maruthuvam, National Institute of Siddha,Tambaram Sanatorium,Chennai-47. 
Type of Sponsor  Research institution and hospital 
 
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 R S Suma  Ayothidoss Pandithar hospital  Room no:7/8, Department of Maruthuvam, National Institute of Siddha, Tambaram Sanatorium, Chennai-47.
Kancheepuram
TAMIL NADU 
9994405417

sumasiddha@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethics Committee   Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: K760||Fatty (change of) liver, not elsewhere classified,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Mandurathi Kudineer  5 Grams bd made into decoction for 90 days 
Comparator Agent  N/A  N/A 
 
Inclusion Criteria  
Age From  20.00 Year(s)
Age To  65.00 Year(s)
Gender  Both 
Details  1.Participants with USG findings suggestive of fatty liver grades I , II, III showing fatty infiltration of the liver 
 
ExclusionCriteria 
Details  1.Participants who are known to consume alcohol[alcohol history taken from participants close relatives]
2.k/c/o chronic kidney diseases, cardiovascular diseases
3.Participants with known liver diseases such as viral hepatitis, autoimmune disorders, biliary disorder, liver abscess, cirrhosis and malignancy
4.Pregnant and lactating women.
5.Participants who have taken drugs that interfere with the lipid metabolism within 3 months before screening such as methotrexate,sodium valporate,amiodarone and glucocorticoids.

 
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
Reduction in the Grades of fatty liver will be assessed by Ultra Sonogram before and after treatment.  6 MONTHS 
 
Secondary Outcome  
Outcome  TimePoints 
1.Changes in Liver function test,lipid profile and fasting blood sugar will be assessed before and after treatment
2.Changes in waist circumference and Body Mass Index will be assessed before and after treatment


 
6 MONTHS 
 
Target Sample Size   Total Sample Size="20"
Sample Size from India="20" 
Final Enrollment numbers achieved (Total)= "0"
Final Enrollment numbers achieved (India)="0" 
Phase of Trial   Phase 2 
Date of First Enrollment (India)   22/06/2024 
Date of Study Completion (India) Date Missing 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Date Missing 
Estimated Duration of Trial   Years="0"
Months="6"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
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
Modification(s)  

 BACKGROUND:

 NON-ALCOHOLIC FATTY LIVER  DISEASE(NAFLD) is the most prevalent chronic liver disease worldwide. Asia being a large, heterogeneous area with substantial variation in socioeconomic status and prevalence of obesity, diabetes mellitus, hypertension, and other metabolic diseases, it has an increasing prevalence of NAFLD with poor outcomincluding hepatocellular carcinoma and death. The prevalence in general population ranges from 11.2% to 37.2%  with a male to  female ratio of 2:1. Increasing sedentary lifestyles and changing dietary patterns plays a major role in the prevalence of this disease. Prevalence of adult NAFLD in the India has been reported between 6.7 and 55.1% of all cases with asymptomatic symptoms of Liver enzymes. 

Non-alcoholic fatty liver disease is defined as fatty liver (FL) that is accumulation of lipids inside the hepatocytes exceeding 5% of  the weight of the liver, without Hepatitis B virus or Hepatitis C virus infection and in the absence of excessive ethanol intake (conventionally defined as an intake of ethanol>20g/day.

 In Siddha literature liver disorders are grouped under “kaleeral Noi”also termed as Maandha katti, Valapaateeral noi and Yagudham. The causes (Noi varum vazhi) of KALEERAL NOI is mentioned as excessive intake of food, taking unhealthy and heavy diets, long term intake of alcoholic beverages.Thus,  the premonitary symptoms  (Murkurikunangal) of KALEERAL NOI, mentioned in the text such as pasiyinmai (anorexia),  seriyamai (indigestion),  suvaiyinmai (tastelessness), kaalaiyil pithamaga vaanthiyadhal (fullness and belching), vaai neer ooral (increased salivary seretion), vayiru naaluku naal peruthal (increased echogenicity of liver due to fatty acid flux),valapaateeral peruthal (hepatomegaly) can be correlated to Non-Alcoholic Fatty Liver Disease. The therapeutic effectiveness of this classical Siddha herbal formulation “MANDURATHI KUDINEER” has not yet been evaluated scientifically,  So, this study makes an  attempt to evaluate its  effectiveness  in an open clinical trial.

OBJECTIVE:

PRIMARY OBJECTIVE:

              To evaluate the therapeutic effectiveness of siddha herbomineral formulation â€œMANDURATHI  KUDINEER” in the management of KALEERAL NOI  (NON-ALCOHOLIC FATTY LIVER DISEASE) by assessment of reduction in the  grades of  fatty liver through USG among the out participants attending  Ayothidoss Pandithar Hospital, National Institute of Siddha.

SECONDARY OBJECTIVE

1         To evaluate the changes in Liver Function Test, lipid profile and fasting blood glucose  of  the  participants

before and after treatment.   

 2. To evaluate the changes in Body Mass Index and Waist circumference of the participants before and after treatment.

METHODOLOGY: 

A total of 20 diagnosed patients of kaleeral noi [ Non alcoholic fatty liver disease ] within the age limit of 20-65 years willing to paticipate in the study by signing the consent form will be enrolled in the study based on the inclusion criteria.

 

PRIMARY OUTCOME:

                                   Reduction in the Grades of fatty liver will be assessed by Ultra Sonogram before and after treatment.

 

SECONDARY OUTCOME:

                                  1.Changes in Liver function test,Lipid profile and Fasting blood sugar will be assessed before and after treatment.

                                  2.Changes in waist circumference and Body mass index will be assessed before and after treatment.

 

RESULTS AND DISCUSSION: The results will be statistically analysed.

KEYWORDS: Kaleeral noi, Non alcoholic fatty liver disease, Mandurathi kudineer, Kudineer.


 
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