| CTRI Number |
CTRI/2024/05/067969 [Registered on: 28/05/2024] Trial Registered Prospectively |
| Last Modified On: |
10/09/2024 |
| Post Graduate Thesis |
No |
| Type of Trial |
Interventional |
|
Type of Study
|
Drug |
| Study Design |
Randomized, Parallel Group, Multiple Arm Trial |
|
Public Title of Study
|
A randomized controlled clinical trial on effect of topical clotrimazole vs. topical fluconazole vs. topical application of gentian violet in the treatment of otomycosis conducted in a tertiary health care centre |
|
Scientific Title of Study
|
A randomized controlled clinical trial on efficacy of topical clotrimazole vs. topical fluconazole vs. topical application of gentian violet in the treatment of otomycosis conducted in a tertiary health care centre |
| Trial Acronym |
NIL |
|
Secondary IDs if Any
|
| Secondary ID |
Identifier |
| NIL |
NIL |
|
|
Details of Principal Investigator or overall Trial Coordinator (multi-center study)
|
| Name |
Dr Srinidhi Ravi |
| Designation |
Assistant Professor |
| Affiliation |
K J Somaiya Medical College |
| Address |
K J Somaiya medical college, Ground floor, opd23, College building, Somaiya Ayurvihar, Sion- Chunabhatti, Mumbai 400022
Mumbai (Suburban) MAHARASHTRA 400022 India |
| Phone |
9699693335 |
| Fax |
|
| Email |
srinidhi.ravi@gmail.com |
|
Details of Contact Person Scientific Query
|
| Name |
Dr Srinidhi Ravi |
| Designation |
Assistant Professor |
| Affiliation |
K J Somaiya Medical College |
| Address |
K J Somaiya medical college, Ground floor, opd23, College building, Somaiya Ayurvihar, Sion- Chunabhatti, Mumbai 400022
Mumbai (Suburban) MAHARASHTRA 400022 India |
| Phone |
9699693335 |
| Fax |
|
| Email |
srinidhi.ravi@gmail.com |
|
Details of Contact Person Public Query
|
| Name |
Dr Srinidhi Ravi |
| Designation |
Assistant Professor |
| Affiliation |
K J Somaiya Medical College |
| Address |
K J Somaiya medical college, Ground floor, opd23, College building, Somaiya Ayurvihar, Sion- Chunabhatti, Mumbai 400022
Mumbai (Suburban) MAHARASHTRA 400022 India |
| Phone |
9699693335 |
| Fax |
|
| Email |
srinidhi.ravi@gmail.com |
|
|
Source of Monetary or Material Support
|
| K J Somaiya Medical College And Hospital, Somaiya Ayurvihar, Everad Nagar, Sion- Chunabhatti, Mumbai, Maharashtra, India. Pincode- 400022 |
|
|
Primary Sponsor
|
| Name |
K J Somaiya Medical College and Hospital |
| Address |
K J Somaiya Medical College and Hospital, Somaiya Ayurvihar, Everad Nagar, Sion- Chunbhatti, Mumbai 400022 |
| Type of Sponsor |
Private medical college |
|
|
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 |
| Dr Srinidhi Ravi |
K J Somaiya Medical College and Hospital |
K J Somaiya Medical College and Hospital , Somaiya Ayurvihar, Everad Nagar, Sion- chunabhatti,Mumbai 400022 Mumbai (Suburban) MAHARASHTRA |
9699693335
srinidhi.ravi@gmail.com |
|
|
Details of Ethics Committee
|
| No of Ethics Committees= 1 |
| Name of Committee |
Approval Status |
| Institutional Ethics Committee Academic K J Somaiya Medical College And Hospital |
Approved |
|
|
Regulatory Clearance Status from DCGI
|
|
|
Health Condition / Problems Studied
|
| Health Type |
Condition |
| Patients |
(1) ICD-10 Condition: H603||Other infective otitis externa, |
|
|
Intervention / Comparator Agent
|
| Type |
Name |
Details |
| Intervention |
Clotrimazole ear drops |
Clotrimazole ear drops will be given to patients with otomycosis for topical use 2 drops thrice a day for 1 week |
| Comparator Agent |
Fluconazole ear drops |
Fluconazole ear drops will be given to patients with otomycosis for topical use 2 drops thrice a day |
| Comparator Agent |
Gentian violet application in external auditory canal |
Gentian violet will be applied topically in external auditory canal of patients with otomycosis by clinician once a week |
|
|
Inclusion Criteria
|
| Age From |
18.00 Year(s) |
| Age To |
75.00 Year(s) |
| Gender |
Both |
| Details |
patients with otomycosis |
|
| ExclusionCriteria |
| Details |
patients with chronic otitis media
patients with history of ear surgery
patients with history of tympanic membrane perforation |
|
|
Method of Generating Random Sequence
|
Computer generated randomization |
|
Method of Concealment
|
Case Record Numbers |
|
Blinding/Masking
|
Participant and Outcome Assessor Blinded |
|
Primary Outcome
|
| Outcome |
TimePoints |
| Earache, aural fullness, ear itching based on visual analogue scale |
baseline, 1 week and 2 weeks |
|
|
Secondary Outcome
|
| Outcome |
TimePoints |
| complete clearance of otomycosis as seen on otoscopy by clinician |
1 week, 2 week follow up |
|
|
Target Sample Size
|
Total Sample Size="100" Sample Size from India="100"
Final Enrollment numbers achieved (Total)= "100"
Final Enrollment numbers achieved (India)="100" |
|
Phase of Trial
|
Phase 3 |
|
Date of First Enrollment (India)
|
10/06/2024 |
| Date of Study Completion (India) |
10/09/2024 |
| Date of First Enrollment (Global) |
Date Missing |
| Date of Study Completion (Global) |
Date Missing |
|
Estimated Duration of Trial
|
Years="0" Months="6" Days="0" |
Recruitment Status of Trial (Global)
Modification(s)
|
Not Yet Recruiting |
| Recruitment Status of Trial (India) |
Completed |
|
Publication Details
|
N/A |
|
Individual Participant Data (IPD) Sharing Statement
|
Will individual participant data (IPD) be shared publicly (including data dictionaries)?
Response - YES
- What data in particular will be shared?
Response - Individual participant data that underlie the results reported in this article, after de-identification (text, tables, figures, and appendices).
- What additional supporting information will be shared?
Response - Study Protocol Response - Informed Consent Form
- Who will be able to view these files?
Response - Researchers whose proposed use of the data has been approved by an independent review committee identified for this purpose.
- For what types of analyses will this data be available?
Response - To achieve aims in the approved proposal.
- By what mechanism will data be made available?
Response - Proposals should be directed to [srinidhi.ravi@gmail.com].
- For how long will this data be available start date provided 01-11-2024 and end date provided 01-11-2029?
Response - Beginning 3 months and ending 5 years following article publication.
- Any URL or additional information regarding plan/policy for sharing IPD?
Additional Information - nil
|
|
Brief Summary
|
RESEARCH QUESTIONS Which antifungal treatment is more efficacious among fluconazole, clotrimazole and topical gentian violet?
HYPOTHESIS There is a significant difference in efficacy among fluconazole, clotrimazole and topical gentian violet. There is no significant difference in efficacy among fluconazole, clotrimazole and topical gentian violet.
AIM To compare efficacy of topical fluconazole, clotrimazole and topical gentian violet in the treatment of otomycosis. METHODOLOGY STUDY DESIGN: Randomized Clinical Trial STUDY SITE: This study will be conducted on patients suffering from Otomycosis coming in the Out patient ENT department (OPD) , K J Sonaiya Medical college and Hospital SAMPLE SIZE: 100 STUDY TIMELINE: 6 months
RESEARCH METHODOLOGY AND ETHICAL CONSIDERATIONS Ethical considerations:
The study will be conducted after obtaining permission from the Institutional Ethics Committee(IEC) All data collected will be strictly confidential and used for the purpose of this study as described below. Written informed valid consent (in English/Hindi/Marathi) will be taken from the subjects before the recruitment of the subjects in this study. Any deviation from the below given methods/procedure will be informed to the Institutional Ethics Committee and only after the IEC’s approval any changes will be made. The Proforma for the written informed consent is given herewith.
Subject Population:
Patients diagnosed with Otomycosis in ENT Out Patient Department will be enrolled in this trial.
Selection criteria:
Male and Female patients above the age of 18 years diagnosed with Otomycosis Patients willing to enrol for the trial meeting the above trial.
EXCLUSION CRITERIA:
Patients not willing to be a part of the study. Patients age below 18 years. Patients having perforated tympanic membrane in the otomycosis infected ear. Patients suffering from Chronic suppurative otitis media(CSOM)/Operated for CSOM
Study procedure:
Enrolment of the patients who fulfil inclusion criteria in the study Recording and documentation of mentioned data collection points as per proforma. Follow up and review patients after 1 week and 2 weeks and check improvement in signs and symptoms. Analysis and interpretation of the data collected.
Patients that present to tertiary health care centre with symptoms of ear pain, itching, discharge, reduced hearing, aural fullness, tinnitus will be asked detailed history and undergo an otoscopic examination. Otomycosis will be confirmed by distinctive otoscopic findings which include: Grayish white mass similar to wet blotting paper. Blackish/white spores in the external auditory canal.
All patients will undergo aural toileting in the OP department itself. Treatment option will be given by Random sampling method. Patients will be asked to pick up a chit among three chits each having name of one of the following drugs ie. Fluconazole, clotrimazole and topical application of gentian violet. Fluconazole and Clotrimazole ear drops will be given as 2 drops three times daily. Patients will be taught proper method of ear drops instillation and to avoid the aggravating factors like water/moisture exposure, use of ear buds, oil instillation. In Group 3 patients receiving topical Gentian violet, solution of Gentian Violet will be applied in the external auditory canal weekly once by the medical practitioner. Other medications including Antihistaminics, Analgesics and Anti-inflammatory drugs will be given as per individual case scenarios and symptoms. Patients will be followed up after 7 days and 14 days for assessing improvement in symptoms and signs for otomycosis.
Data collection and Analysis:
All data will be collected in google sheets and printed form in the form of a specific proforma for the study. Appropriate statistical tests - Chi square test will be applied to analyse the data as necessary.
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