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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  
Name  Address 
NIL  NIL 
 
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 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
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
 
 
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 
Publication Details    
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     

 
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