None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Subjects belonging to the age group of 20 – 40 years, of either gender. 2. Subjects who fulfil the criteria of premature ageing based on the symptoms mentioned in classical texts and similar questionnaires. (available validated questionnaire/ formulation of a validated tool) 3. Subjects who are willing to provide written consent to participate in the study and give 3-5 ml of blood sample for biochemical test.
Exclusion criteria
Exclusion criteria: 1. Subjects with uncontrolled diabetes, hypertension, hypothyroidism and severe obesity. 2. Subjects with any unstable heart disease or known case of MI or unstable angina. 3. Individuals with any type of addiction such as tobacco, smoking, alcohol, substance abuse. 4. Currently the pregnant or post-partum state of lactating women. 5. Subjects who have completed participation in any other clinical trial during past six months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.Improvement in subjective parameters of premature ageing (assessed by questionnaire).Timepoint: 56 days | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Improvement in the following markers of Oxidative stress namely, Nitric Oxide (NO), Glutathione (GSH) and Malondialdehyde (MDA).Timepoint: 56 days | — |
Countries
India
Contacts
Ayurvedic and Unani Tibbia College and Hospital