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Study of host immune response in patients of fungal infection of skin.

Comparative evaluation of host immune response and cytokine signature pertaining toTh1 and Th2 immune arms in serum and tissue among patients of acute localized versus chronic disseminated dermatophytosis, hospital based observational study. - None

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2019/09/021297
Enrollment
236
Registered
2019-09-17
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: B356- Tinea cruris

Interventions

None listed

Sponsors

Indian Association of Dermatologists Venereologists and Leprologists
Lead Sponsor
GCS Medical College Hospital and Research Centre
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of either sex age between 18 to 60 years. 2. Skin condition clinically diagnosed as dermatophytosis involving non glabrous skin (exluding tinea unguim and tinea capitis) 3. Presence of fungus in scrapping taken from lesion by in KOH preparation. 4. Women of child bearing age must have a negative urine pregnancy test. 5. Patient willing to give written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patient less than 18 years age and more than 60 years.(DOB, govt approved document in case of doubt) 2. Preexisting Cardiovascular, pulmonary, hepatic, renal, hematological, gastrointestinal, endocrine, immunologic, musculoskeletal, neurological or psychiatric disease.(History and medical record) 3. Major surgical or medical illness in last 4 weeks before screening.(History and medical record) 4. Any concomitant medication for purpose other than dermatophytosis management at presentation or within last 4 weeks before screening. (History and medical record). 5. Patient with concommitent asthma, atopic dermatitis allergic rhinitis. Patient with past history of same documented on medical records will also be exluded from study. 6. Patients on corticosteroid or have taken same during last 4 weeks. 7. Patinets who are on at present or treated during last 6 months with any biologic medication.

Design outcomes

Primary

MeasureTime frame
1. Study of quantitative levels of IFN- γ in serum and expression of same in skin biopsies (using immunohistochemistry (IHC) in paraffin embaded tissue) in patient of dermatophytosis in both study groups. 2. Study of quantitative levels of IL-4 in serum and expression of same in skin biopsies(using IHC in paraffin embaded tissue) in patient of dermatophytosis in both study groups. 6. To study effect of â??priore use of topical or systemic steroidâ?? on study parameters in both group. Timepoint: end of study

Secondary

MeasureTime frame
1. Identificaiton of species of dermatophytosis in both study groups. 2. To study difference in cytokine profile in serum and tissue in both group in relation to mycological species identified. Timepoint: end of study

Countries

India

Contacts

Public ContactDr Nayankumar H Patel

GCS Medical College, Hospital & Research Centre.

patelnayan78.np@gmail.com9925011309

Outcome results

None listed

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