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A study of effect of immunity boosting therapy on long-standing ringworm infections

Immunotherapy with purified protein derivative(PPD)in the management of chronic,recurrent or relapsing dermatophytosis: A,hospital based,interventional ,randomised,double blind comparative,study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/10/021656
Enrollment
100
Registered
2019-10-15
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: L089- Local infection of the skin and subcutaneous tissue, unspecified

Interventions

Intervention1: purified protein derivative(10 TU/0.1ml): Injection of 0.1 ml of purified protein derivative(10 TU/0.1ml) intradermally into the deltoid area of alternate arm,every 15 days for a total

Sponsors

GCS Medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of either sex, aged more than 18 years ,suffering from chronic and relapsing dermatophytosis,confirmed by positive 10% potassium hydroxide mount for fungal hyphae

Exclusion criteria

Exclusion criteria: 1. Pregnant and lactating females 2. Patients with liver or renal failure or any malignancy 3. Patients with primary or acquired immunodeficiency 4. Patients with any major medical illness or surgical intervention within the preceding 4 weeks 5. Patients on concomitant medications which can interfere with immune response(eg steroids,immunosuppressants,chemotherapeutic agents) 6. Patients with a past history of tuberculosis

Design outcomes

Primary

MeasureTime frame
All the patients in both the groups shall be assessed for 1 Complete Clearance of the dermatophytosis(assessed by Grade of improvement scoring,physicians and patientsglobal assessment score) at the end of 8 weeks 2) Reduction in the Itch score at the end of 8 weeks 3) Percentage of patients have having clinical relapse at 4,8,12 weeks after the last Intradermal PPD injection Timepoint: 1 Complete clearance of the infection at 8 weeks 2 Absence of relapse at 12 and 20 weeks

Secondary

MeasureTime frame
1) Correlation of serum IgE levels and personal and family history of atopy with the primary outcome measures. 2) Correlation of preceding topical steroid use with the primary outcome parameters 3) Correlation of pre-study PPD positivity with the primary outcome measures. Timepoint: 8 and 20 weeks

Countries

India

Contacts

Public ContactDr Kalgi Baxi

GCS Medical college and hospital

patelnayan78.np@gmail.com9925011309

Outcome results

None listed

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