A study to validate smart breath analyzer as a screening tool for diabetic, hepatic, renal, lung, lipid and othermetabolic disorders

Not Applicable

• Conditions: Health Condition 1: E888- Other specified metabolic disorders

• Registration Number: CTRI/2022/09/045983
• Lead Sponsor: Humors Tech Pvt Ltd

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 6 February 2023

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1. Participant must either be a completely healthy individual as confirmed by blood examination or a known case of diseases in focus such as diabetes, kidney issue, liver issue, lung issue and lipid issue with relevant diagnostics reports tested within 15 days of participation in the study.

a. Patients that are known case of Diabetes tested for FBS or RBS within 15 days of participation

b. Patients that are known case of kidney related disease tested for RFT within 15 days of participation

c. Patients that are known case of liver related disease tested for LFT within 15 days of participation

d. Patients that are known case of lung related disease tested by spirometry within 15 days of participation

e. Patients that are known case of lipid related disease tested for lipid profile within 15 days of participation.

2. All genders, ethnicity

3. Age Group: 18 to 75years

4. Participant who has given informed consent for participating in this study

5. Participant must be fully vaccinated for COVID

6. Participant must use smart breath analyzer at fasting condition. If not fasting, there should be a minimum gap of 1 hour between consuming water and testing, and 3-4 hours between consuming food and testing.

Exclusion Criteria

1. Individual less than 18 or above 75years of age

2. Pregnant and lactating females

3. Known case of ongoing illness such as

a. Cancer

b. AIDS

c. COVID

d. Cough, Fever

e. TB

f. Chickenpox

g. Influenza

h. Mumps

i. Tonsil

4. Individual who has not given informed consent for this study

Study & Design

• Study Type: Observational
• Study Design: Not specified