| 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
|
|
|
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
|
|
|
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 Noiâ€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 “MANDURATHI 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. |