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Clinical Trials/CTRI/2021/06/034341
CTRI/2021/06/034341
Completed
未知

Efficacy, Safety and Quality of Life with different Itraconazole regimens in Recurrent Tinea Corporis and Tinea Cruris: An Interventional Study

Pt BD Sharma PGIMS Rohtak0 sites72 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: L088- Other specified local infections of the skin and subcutaneous tissue
Sponsor
Pt BD Sharma PGIMS Rohtak
Enrollment
72
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
March 29, 2023
Last Updated
3 years ago
Study Type
Interventional

Investigators

Sponsor
Pt BD Sharma PGIMS Rohtak

Eligibility Criteria

Inclusion Criteria

  • 1\. Patient 18\-65 years of age of either gender
  • 2\. Patient who has recurrence of lesions of tinea corporis and tinea cruris in less than 6 weeks after clinical cure
  • 3\. Patient willing to provide written informed consent.
  • 4\. Patients willing to come for regular follow up.

Exclusion Criteria

  • 1\. Patient who has recurrence of lesions of tinea corporis and tinea cruris in less than 6 weeks after completion of treatment with Itraconazole and having been cured clinically.
  • 2\. Patient suffering from tinea infections other than tinea corporis and tinea cruris.
  • 3\. Patients with a history of intolerance or hypersensitivity to the study drugs.
  • 4\. Patients who have serious concomitant illness which can prevent the completion of study.
  • 5\. Patients with contact dermatitis, atopic dermatitis, psoriasis or any other skin disease.
  • 6\. All pregnant and breastfeeding females.
  • 7\. Patients with hepatic, renal or cardiac disease.
  • 8\. Patients on drugs that are contraindicated for use with itraconazole, which include pimozide, dofetilide, quinidine, oral midazolam, triazolam, nisoldipine, felodipine, dihydroergotamine, ergotamine, ergometrine, methylergometrine, cisapride, lovastatin, simvastatin, levacetylmethadol, and methadone.

Outcomes

Primary Outcomes

Not specified

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