A study to compare salivary adiponectin and salivary pH in type 2 diabetes patients and healthy individuals of different weight categories
- Conditions
- Health Condition 1: E119- Type 2 diabetes mellitus without complications
- Registration Number
- CTRI/2020/04/024619
- Lead Sponsor
- Jamia Hamdard
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1. Subject must be a male or female of the age group 18-60 years.
2. Subject must have confirmed diagnosis of T2DM.
3. Subject having Body Mass Index (BMI) >= 18kg/m2.
4. Subject capable of giving informed consent.
5. Subject willing to participate in the study.
1. Subject having hypertension and/or pulmonary disease.
2. Subject having kidney disease, liver disease, or malignancy.
3. Subject having recent acute illness.
4. Subject having severe cognitive decline and/or Alzheimer dementia.
5. Subject having a history of depression.
6. Subject having drugs or alcohol abuse or dependence in the last two years.
7. Lactating or pregnant subject.
8. Subjects who complain of dry mouth or dry eyes.
9. Subject having open wounds and/or sores in their mouths.
10. Subject having any recent dental surgery.
11. Subject unable to give informed consent.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the salivary adiponectin levels and salivary pH of type 2 diabetics and healthy volunteers of different weight classes (obese/overweight and normal weight)Timepoint: Once
- Secondary Outcome Measures
Name Time Method To compare the salivary adiponectin levels to the cognitive function assessed by using MoCA test.Timepoint: Once