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Use of Halometasone in skin diseases caused by occupational exposure to different agents.

Halometasone monohydrate 0.05% in occupational contact dermatitis: A clinicoepidemiological study - HALOCD

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2014/08/004876
Enrollment
150
Registered
2014-08-13
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Occupational contact dermatitis (both irritant and allergic)

Interventions

Intervention1: Halometasone monohydrate 0.05%: After baseline assessments, patients will be advised to apply commercially available Halometasone 0.05% ointment twice daily locally as a thin layer over

Sponsors

SELF
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • All patients with pruritic eczematous conditions that started or aggravated for the first time after joining the present occupation will be included. The diagnosis of occupational contact dermatitis will be done based on taking detailed medical and occupational history and the presence of clinical signs and symptoms including pruritus and eczema. • Lesions over all areas, including exposed as well as covered areas, will be included unless they are solely restricted to covered areas/ groins or genitalia.

Exclusion criteria

Exclusion criteria: • The diseases excluded were infective diseases like scabies, fungal infections, bacterial infections and all noneczematous dermatoses like psoriasis and lichen planus, even if associated with itching. • Lesions solely affecting the groins, genitals or covered areas. • Patients who are already under treatment for the presenting conditions. • Patients with history of hypersensitivity to topical steroids. • Patients (including severe/extensive eczema) in need of any form of treatment that influences the healing of the lesion such as topical treatment other than trial preparation, topical radiation therapy, systemic medication with antibiotics, antimicrobials, antihistaminics, cytostatics, corticosteroids, or ACTH will also be excluded. • Pregnant and nursing women, patients with history of cardiovascular, hematological, pancreatic, metabolic, neurological, or clinically significant laboratory abnormalities which would interfere with patient participation in the study or evaluation of patientâ??s response to therapy were excluded from screening.

Design outcomes

Primary

MeasureTime frame
SCORAD (SCORing Atopic Dermatitis) IndexTimepoint: At 2 weeks and 4 weeks

Secondary

MeasureTime frame
â?¢IGA (Investigatorâ??s Global Assessment) scale â?¢POEM (Patient Oriented Eczema Measure) â?¢DQLI (Dermatology Life Quality Index)Timepoint: At 2 weeks and 4 weeks

Countries

India

Contacts

Public ContactRITUPARNA MAITI

AIIMS, Bhubaneswar

rituparnamaiti@gmail.com09438884191

Outcome results

None listed

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