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An observation study to see the effect of incompatible diet in development of shvitra(vitiligo)

Evaluating classical etiopathogenesis of Shvitra (Vitiligo) in current era in relation to Prakriti and Biochemical Markers-A case control study.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/02/030941
Enrollment
160
Registered
2021-02-02
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: L80- Vitiligo

Interventions

None listed

Sponsors

All India institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient presenting with symptoms of SHVITRA (vitiligo) will included in this study. 2.Patient will be randomly selected irrespective of sex, age, religion, occupation, and economic status after due processed of informed consent. 3. Patient will be randomly selected irrespective of origin, site, size of patches. 4.Patients between the age group of 10 to 60 years. 5.Less than 1-3 year diagnosed case.

Exclusion criteria

Exclusion criteria: 1.Noncooperative and immunosuppressive patient. 2.Patient below 10year and above 60 year. 3.Pregnent women. 4.Patient with history of burn and trauma.

Design outcomes

Primary

MeasureTime frame
To prepare preventive protocol for SHVITRA (vitiligo). ,To identify which prakriti is more prone to develop SHVITRA (vitiligo) , To identify biochemical markers (based on rakta dusti and virudha aahara) in pt. of SHVITRA. Timepoint: 1 year

Secondary

MeasureTime frame
o prepare preventive protocol for SHVITRA (vitiligo). ,To identify which prakriti is more prone to develop SHVITRA (vitiligo) ,To identify biochemical markers (based on rakta dusti and virudha aahara) in pt. of SHVITRA. Timepoint: 1 year

Countries

India

Contacts

Public ContactDr Anand more

All India institute of Ayurveda

drmoreanand@gmail.com8830389544

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026