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Clinical Trials/CTRI/2019/01/017033
CTRI/2019/01/017033Not yet recruitingNot Applicable

Prevalence of Allergic contact dermatitis using patch testing in nurses in tertiary care hospital

MGM MEDICAL COLLEGE AND HOSPITAL1 site in 1 country326 target enrollmentStarted: January 18, 2019Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
326
Locations
1
Primary Endpoint
prevalence of allergic contact dermatitis using patch testing in nurses in tertiary care hospital

Study Overview

Brief Summary

Prevalence studies reveal dermatitis is about 20% of the general population at one time. Hand dermatitis is present in about 2% of the people at any time with a lifetime risk of 20% in women. Contact dermatitis makes up to 80% of all occupational skin disease

Nurses are at very high risk for dermatitis because of exposure to potential irritants, including glove wearing, alcohol rub use, hand washing with water and disinfectants. as the prevalence of allergic contact dermatitis is rapidly increasing among nurses, and there is lack of awareness among them with lack of many research done on nurses, it should be considered a priority with interventional strategies to reduce its prevalence.

Bajaj A K, Saraswat A, Mukhjia G, Rastogi S, Yadav S "Patch testing experience with 1000 patients " Indian J Dermatol Venerol Leprol 2007;73:313-8

Bhattarai S, Agarwal S, Rijal A." Clinical and contact allergolocial observation on Hand Eczema: A Descriptive study " Current allergy & clinical immunology 2014 Nepal Med Coll J 2014; 16(1): 37-41

Study Design

Study Type
Observational

Eligibility Criteria

Ages
18.00 Year(s) to 57.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • 1 All the nurses working in MGM Medical college and hospital, Aurangabad having hand eczema.

Exclusion Criteria

  • 1 Any active lesion present -erythema, vesicles, edema etc 2 Pregnant women 3 Lactating women.

Outcomes

Primary Outcomes

prevalence of allergic contact dermatitis using patch testing in nurses in tertiary care hospital

Time Frame: patient will be followed up after 48 hours followed by 96 hours

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Private medical college

Study Sites (1)

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