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Clinical Trials/CTRI/2022/12/048189
CTRI/2022/12/048189CompletedNot Applicable

A community-based study of prevalence of skin disorders in semi-urban and urban Telangana State

Pfizer Inc1 site in 1 country2,000 target enrollmentStarted: February 1, 2023Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Pfizer Inc
Enrollment
2,000
Locations
1
Primary Endpoint
we aim to determine the prevalence of skin disorders in urban and semi urban communities and their impact on quality of life.

Study Overview

Brief Summary

Skin diseases contributed about 2% of the global burden of diseases measured in Disease Adjusted Life Years (DALYs) (1). The prevention and management of skin diseases received less attention in the past decades due to low mortality rates. However, a recent Global Burden of Disease Study finding revealed that skin diseases rank 18 in top 20 diseases in terms of DALYs and is fourth leading cause of nonfatal disease burden (2). Further, skin diseases increase clinical depression and anxiety. The prevalence and pattern of skin diseases are influenced by the overall ecosystem of the region including sociocultural milieu, topography, nutrition, genetics etc.

In India, skin diseases have been profiled through hospital-based studies with low levels of prevalence (3-7) as compared to community-level. The prevalence varied from 4.2% to 11.6% in the general population. However, high prevalence has been reported (30%–40%) in pediatric population (8, 9) and 60% in a community-based survey in the central India (10). There is a dearth of data about prevalence in skin diseases among semi-urban/rural communities in Telangana.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
2.00 Year(s) to 99.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • 1.Subjects age 2 years and above 2.Subjects who have skin disorders 3.Able to provide informed consent/ assent (in case of children).
  • 4.Subjects who reside in the study area (for at least 6 months).

Exclusion Criteria

  • 1.Subjects with no skin disorders.
  • 2.Subjects below the age of 2 years 3.Subjects unable to participate in study related procedures 4.Subjects unwilling or unable to provide informed consent/assent 5.Subjects who do not reside in the area (at 6 months) and/or are unlikely to reside in the area until end of December 2023.

Outcomes

Primary Outcomes

we aim to determine the prevalence of skin disorders in urban and semi urban communities and their impact on quality of life.

Time Frame: 12 to 13 months

Secondary Outcomes

  • •To determine impact on quality of life due to skin disorders(•To explore influence of predisposing conditions including influence of geography on skin disorders and quality of life)

Investigators

Sponsor
Pfizer Inc
Sponsor Class
Pharmaceutical industry-Global

Study Sites (1)

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