Please note that the copy function is not enabled for this field.
If you wish to
modify
existing outcomes, please copy and paste the current outcome text into the Update field.
LOGIN
CREATE ACCOUNT
LOGIN
CREATE ACCOUNT
MY TRIALS
REGISTER TRIAL
FAQs
HINTS AND TIPS
DEFINITIONS
Trial Review
The ANZCTR website will be unavailable from 1pm until 3pm (AEDT) on Wednesday the 30th of October for website maintenance. Please be sure to log out of the system in order to avoid any loss of data.
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this
information for consumers
Download to PDF
Trial registered on ANZCTR
Registration number
ACTRN12608000235303
Ethics application status
Approved
Date submitted
6/05/2008
Date registered
8/05/2008
Date last updated
16/10/2008
Type of registration
Retrospectively registered
Titles & IDs
Public title
Topical capsaicin in burning mouth syndrome
Query!
Scientific title
The efficacy of topical capsaicin in reducing symptoms in patients with burning mouth syndrome
Query!
Universal Trial Number (UTN)
Query!
Trial acronym
BMS capsaicin
Query!
Linked study record
Query!
Health condition
Health condition(s) or problem(s) studied:
burning mouth syndrome
3123
0
Query!
Condition category
Condition code
Oral and Gastrointestinal
3287
3287
0
0
Query!
Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
Query!
Intervention/exposure
Study type
Interventional
Query!
Description of intervention(s) / exposure
Patients will be instructed to apply topical capsaicin 0.075%, twice a day (middle morning and middle afternoon) for 8 weeks with a one-week interval - the fourth.
Query!
Intervention code [1]
2869
0
Treatment: Drugs
Query!
Comparator / control treatment
The control group received placebo - the water based cream utilized as vehicle for the capsaicin, twice a day, 4 weeks.
Query!
Control group
Placebo
Query!
Outcomes
Primary outcome [1]
4174
0
relief of symptoms assessed through a visual analogue scale and a questionnaire of an overall effect perceived
Query!
Assessment method [1]
4174
0
Query!
Timepoint [1]
4174
0
4 weeks after starting medication or placebo, 8 weeks at the ending of drug administration and 12 weeks, four weeks after drug discontinuation.
Query!
Secondary outcome [1]
7049
0
lasting of the benefits achieved - relief of symptoms, measured through visual analogue scale and a questionnaire of an overall effect perceived
Query!
Assessment method [1]
7049
0
Query!
Timepoint [1]
7049
0
six months after discontinuation of drug treatment
Query!
Eligibility
Key inclusion criteria
burning mouth syndrome, no recent use of other drugs
Query!
Minimum age
Not stated
Query!
Query!
Maximum age
Not stated
Query!
Query!
Sex
Both males and females
Query!
Can healthy volunteers participate?
No
Query!
Key exclusion criteria
diabetic patients, anemia, candida infection
Query!
Study design
Purpose of the study
Treatment
Query!
Allocation to intervention
Non-randomised trial
Query!
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Query!
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Query!
Masking / blinding
Blinded (masking used)
Query!
Who is / are masked / blinded?
Query!
Query!
Query!
Query!
Intervention assignment
Parallel
Query!
Other design features
Query!
Phase
Phase 3
Query!
Type of endpoint/s
Safety/efficacy
Query!
Statistical methods / analysis
Query!
Recruitment
Recruitment status
Completed
Query!
Date of first participant enrolment
Anticipated
10/12/2007
Query!
Actual
Query!
Date of last participant enrolment
Anticipated
Query!
Actual
Query!
Date of last data collection
Anticipated
Query!
Actual
Query!
Sample size
Target
20
Query!
Accrual to date
Query!
Final
Query!
Recruitment outside Australia
Country [1]
961
0
Brazil
Query!
State/province [1]
961
0
Sao Paulo
Query!
Funding & Sponsors
Funding source category [1]
3365
0
University
Query!
Name [1]
3365
0
Sao Paulo University
Query!
Address [1]
3365
0
Prof Lineu Prestes Av, 2227 Sao Paulo
PC 05508-000
Query!
Country [1]
3365
0
Brazil
Query!
Primary sponsor type
University
Query!
Name
Sao Paulo University
Query!
Address
Prof Lineu Prestes Av, 2227 Sao Paulo
PC 05508-000
Query!
Country
Brazil
Query!
Secondary sponsor category [1]
3012
0
Government body
Query!
Name [1]
3012
0
Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)
Query!
Address [1]
3012
0
Ministerio da Educacao, anexos I e II, Brasilia, DF, PC 70359-970
Query!
Country [1]
3012
0
Brazil
Query!
Ethics approval
Ethics application status
Approved
Query!
Ethics committee name [1]
5383
0
Sao Paulo University, School of Dentistry Ethics Committee
Query!
Ethics committee address [1]
5383
0
Prof Lineu Prestes Av, 2227 Sao Paulo PC 05508-000
Query!
Ethics committee country [1]
5383
0
Brazil
Query!
Date submitted for ethics approval [1]
5383
0
Query!
Approval date [1]
5383
0
10/08/2007
Query!
Ethics approval number [1]
5383
0
Query!
Summary
Brief summary
Query!
Trial website
Query!
Trial related presentations / publications
Query!
Public notes
Query!
Contacts
Principal investigator
Name
28569
0
Query!
Address
28569
0
Query!
Country
28569
0
Query!
Phone
28569
0
Query!
Fax
28569
0
Query!
Email
28569
0
Query!
Contact person for public queries
Name
11726
0
norberto nobuo sugaya
Query!
Address
11726
0
Prof Lineu Prestes Av, 2227 Sao Paulo
PC 05508-000
Query!
Country
11726
0
Brazil
Query!
Phone
11726
0
55 11 30917883
Query!
Fax
11726
0
55 11 30917883
Query!
Email
11726
0
[email protected]
Query!
Contact person for scientific queries
Name
2654
0
bianca fréo
Query!
Address
2654
0
Prof Lineu Prestes Av, 2227 Sao Paulo
PC 05508-000
Query!
Country
2654
0
Brazil
Query!
Phone
2654
0
55 11 98908221
Query!
Fax
2654
0
Query!
Email
2654
0
[email protected]
Query!
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
Download to PDF