Manikkadai Nool Measurement height, weight, wrist and waist circumference measurement for patients with Diabetes,Obesity, hypertensio

Not Applicable

Completed

• Conditions: Health Condition 1: E669- Obesity, unspecified

• Registration Number: CTRI/2021/02/030903
• Lead Sponsor: The Director General

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2023-03-07
• Last Update Posted: 3 April 2023

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 80

Inclusion Criteria

Both sex, aged between 19-60 yrs.

Presence of three out of the five of the following criteria constituted a diagnosis of the MS in accordance with the modified NCEP ATP III recommendations as mentioned below:

(1)WC > 102 cm in men or 88 cm in women

(2)Fasting TG >= 1.7 mmol/l

(3)HDL-C < 1.0 mmol/l in men or <1.3 mmol/l in women

(4)Blood pressure >= 130/85 mmHg or hypertensive on medication (5) Fasting glucose >= 6.0 mmol/l.

Patients with history of Metabolic Syndrome irrespective of the underlying etiology like life style disorder or any endocrine disorders.

Healthy Volunteers to be selected based on their clinical history stating the absence of criteria mentioned under modified NCEP ATP III criteria for MetS and history of any other illness.

Exclusion Criteria

Patients below 19 yrs of age and above 61yrs.

Patients with clinical presentations or with history of infectious illness and are under treatment for the same.

Patients with clinical history of emaciating illness like Carcinoma, H/o Chronic Kidney Disease, Liver cirrhosis, Ascites of any etiology.

Subjects with congenital or acquired physical deformity that could interrupt measuring Manikkadai Nool measurement.

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The resemblance of Manikkadai Nool measurements in subjects with Metabolic Syndrome with measurements related to clinical symptoms mentioned in the classical text.Timepoint: 6 months

Secondary Outcome Measures

Name	Time	Method
To find out the variations in the Manikkadai Nool measurement based on the hematologic parameters of every individual. <br/ ><br>To document variations in Manikkadai Nool measurement based on the Anthropometric measures.Timepoint: Period that may be required for analyzing the data and data data compilation is 3 months