| CTRI Number |
CTRI/2022/12/047904 [Registered on: 06/12/2022] Trial Registered Prospectively |
| Last Modified On: |
04/12/2022 |
| Post Graduate Thesis |
Yes |
| Type of Trial |
Interventional |
|
Type of Study
|
Drug |
| Study Design |
Randomized, Parallel Group Trial |
|
Public Title of Study
|
A study to compare the benefits between itraconazole and terbinafine with itraconazole in skin fungal infections |
|
Scientific Title of Study
|
A prospective, randomized, open label, comparative study of efficacy & tolerability of oral itraconazole versus combination therapy with oral itraconazole & oral terbinafine in treatment of dermatophytosis
|
| Trial Acronym |
|
|
Secondary IDs if Any
|
| Secondary ID |
Identifier |
| NIL |
NIL |
|
|
Details of Principal Investigator or overall Trial Coordinator (multi-center study)
|
| Name |
Srinjoy Bhattacharya |
| Designation |
Postgraduate in Pharmacology |
| Affiliation |
Kempegowda Institute of Medical Sciences |
| Address |
KIMS Mens hostel
Banashankari 2nd stage
Department of Dermatology
KR Road Bangalore KARNATAKA 560070 India |
| Phone |
9620168753 |
| Fax |
08027612798 |
| Email |
srinjoyb94@gmail.com |
|
Details of Contact Person Scientific Query
|
| Name |
Girish K |
| Designation |
Professor |
| Affiliation |
Kempegowda Institute of Medical Sciences |
| Address |
KIMS college
Department of Pharmacology
Bangalore KARNATAKA 560070 India |
| Phone |
9980911060 |
| Fax |
|
| Email |
drgirish_k@rediffmail.com |
|
Details of Contact Person Public Query
|
| Name |
Srinjoy Bhattacharya |
| Designation |
Postgraduate in Pharmacology |
| Affiliation |
Kempegowda Institute of Medical Sciences |
| Address |
Kims Mens hostel
Banashankari stage 2 Department of Dermatology
KR Road Bangalore KARNATAKA 560070 India |
| Phone |
9620168753 |
| Fax |
08027612798 |
| Email |
srinjoyb94@gmail.com |
|
|
Source of Monetary or Material Support
|
| Kempegowda Institute of Medical Sciences
Hospital and Research Centre
Department of Dermatology
|
|
|
Primary Sponsor
|
| Name |
nil |
| Address |
nil |
| Type of Sponsor |
Other [Academic study] |
|
|
Details of Secondary Sponsor
|
|
|
Countries of Recruitment
|
India |
|
Sites of Study
|
| No of Sites = 1 |
| Name of Principal
Investigator |
Name of Site |
Site Address |
Phone/Fax/Email |
| srinjoy bhattacharya |
Kempegowda Institute of Medical Sciences Hospital and Research Centre |
Department of Dermatology
K.R road, vishweshwarapura, bangalore, karnataka -560002
Bangalore KARNATAKA |
9620168753
srinjoyb94@gmail.com |
|
|
Details of Ethics Committee
|
| No of Ethics Committees= 1 |
| Name of Committee |
Approval Status |
| Institutional Ethics Committtee Kempegowda Institute of Medical Sciences |
Approved |
|
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Regulatory Clearance Status from DCGI
|
|
|
Health Condition / Problems Studied
|
| Health Type |
Condition |
| Patients |
(1) ICD-10 Condition: B359||Dermatophytosis, unspecified, |
|
|
Intervention / Comparator Agent
|
| Type |
Name |
Details |
| Intervention |
Oral itraconazole |
Oral itraconazole 100 mg twice daily for 3 weeks |
| Comparator Agent |
Oral itraconazole plus oral terbinafine |
Oral itraconazole 100 mg twice daily plus oral terbinafine 250 mg once daily for 3 weeks |
|
|
Inclusion Criteria
|
| Age From |
18.00 Year(s) |
| Age To |
65.00 Year(s) |
| Gender |
Both |
| Details |
Subjects aged between 18-65 years of age with clinical diagnosis of dermatophytosis(tinea corporis,tinea faciei,tinea cruris) including all new cases & recurrent cases of dermatophytosis
|
|
| ExclusionCriteria |
| Details |
Pregnant & lactating women
Subjects with history of preexisting liver & renal disease
Subjects with history of HIV or under antiretroviral therapy
Subjects with history of hypersensitivity to the drugs under study
Subjects under immunosuppressive therapy
|
|
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Method of Generating Random Sequence
|
Coin toss, Lottery, toss of dice, shuffling cards etc |
|
Method of Concealment
|
Not Applicable |
|
Blinding/Masking
|
Open Label |
|
Primary Outcome
|
| Outcome |
TimePoints |
Itching
Erythema
Scaling
|
At baseline,3,6 and 9 weeks |
|
|
Secondary Outcome
|
| Outcome |
TimePoints |
Any side effects like GI disturbances, headache, rashes, allergic symptoms
|
0,3,6 and 9 weeks |
|
|
Target Sample Size
|
Total Sample Size="150" Sample Size from India="150"
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" |
|
Phase of Trial
|
N/A |
|
Date of First Enrollment (India)
|
07/12/2022 |
| Date of Study Completion (India) |
Applicable only for Completed/Terminated trials |
| Date of First Enrollment (Global) |
Date Missing |
| Date of Study Completion (Global) |
Applicable only for Completed/Terminated trials |
|
Estimated Duration of Trial
|
Years="1" Months="6" Days="0" |
|
Recruitment Status of Trial (Global)
|
Not Yet Recruiting |
| Recruitment Status of Trial (India) |
Not Yet Recruiting |
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Publication Details
|
|
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Individual Participant Data (IPD) Sharing Statement
|
Will individual participant data (IPD) be shared publicly (including data dictionaries)?
Response - NO
|
|
Brief Summary
|
Superficial dermatophytosis is a common dermatosis in clinical practice. They affect skin, hair, nails and are called ‘tinea’ based on the area of involvement. e.g. Tinea pedis/foot, Tinea cruris/groin, Tinea corporis or ringworm in the body, Tinea faciei/Face, Tinea capitis/Scalp They are generally responsive to topical antifungal agents such as Miconazole, Terbinafine and Butenafine cream, but oral antifungals are indicated for extensive infections, immunocompromised patients and failed topical treatment with Itraconazole, Terbinafine, Griseofulvin, Fluconazole. The use of Ketoconazole has been limited due to risk of hepatotoxicity. Griseofulvin rapidly clears from the stratum corneum, so it carries the risk of relapse Fluconazole and Terbinafine are effective but can be used short term or even pulse regimes for treating various superficial fungal infections. Itraconazole has shown good results in treatment of dermatophytosis at doses of 100mg once a day for 2 weeks and with 200 mg once a day for 1 week. Because of frequent relapses at short intervals, physicians prefer using it in doses of 100mg BID/ 200 mg once a day for prolonged periods. Terbinafine was considered to be first line drug (250mg OD for 2 weeks) for treatment of Tinea infections. However recently reports of terbinafine resistance with therapeutic failures and relapses have come up. Terbinafine was reported to be efficacious and safe in dermatophytosis with fewer therapeutic failure rates at doses of 500 mg/day. Over the years, the morphology, course and treatment of Tinea in India has undergone some significant changes. Sufficient data about effectiveness of Oral antifungals is lacking. Although comparative studies have been done among individual drugs, there are limited studies available in India to compare the safety and efficacy of monotherapy with combination therapy of study drugs. Objectives of the study: To compare the efficacy & tolerability of monotherapy using oral itraconazole with combination therapy of oral itraconazole & oral terbinafine in treatment of dermatophytosis(tinea corporis ,tinea cruris ,tinea faciei) . Materials and Methods- Group A - Oral itraconazole 100 mg BID for 3 weeks Group B - Oral itraconazole 100 mg BID & oral terbinafine 250 mg OD for 3 weeks Follow up visits- Done at 3 weeks, 6 weeks and 9 weeks. • At each visit, following clinical parameters will be assessed using a 4-point scale • Itching • Erythema • Scaling • 0 = none; 1 = mild; 2 = moderate; 3 = severe • Clinical cure = erythema & scaling grade 0 & itching grade 0 or 1 • Mycological cure = Negative KOH smear • At the end of 3 weeks, subjects who show relapse or partial clinical recovery will be administered with oral Itraconazole 100 mg BID for additional 3 weeks as rescue medication. • Tolerability parameters: Whether subjects experience any side effects like GI disturbances, headache, rashes, allergic symptoms |