Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12617000877381
Ethics application status
Approved
Date submitted
13/06/2017
Date registered
15/06/2017
Date last updated
29/06/2022
Date data sharing statement initially provided
13/12/2018
Type of registration
Prospectively registered

Titles & IDs
Public title
METHODS - A randomised controlled trial of METhotrexate to treat Hand Osteoarthritis
with Synovitis
Scientific title
METHODS - A randomised controlled trial of METhotrexate to treat Hand Osteoarthritis
with Synovitis
Secondary ID [1] 292186 0
NHMRC Project Grant APP1127981
Universal Trial Number (UTN)
Trial acronym
METHODS
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Hand osteoarthritis with synovitis 303660 0
Condition category
Condition code
Musculoskeletal 303049 303049 0 0
Osteoarthritis

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Methotrexate
- the dose administered: 10 mg weekly for four weeks, followed by 20 mg weekly for the remainder of the study if there is no toxicity as determined at the physician’s discretion (Australian Rheumatology Association Guidelines)
- the duration of administration: 6 months
- the mode of administration: oral tablet

All participants will be prescribed oral folic acid at a minimum dose of 5 mg/week, 6 days/week.

Pill count will be performed at 4 weeks, 3 and 6 months after randomisation to monitor adherence.
Intervention code [1] 298345 0
Treatment: Drugs
Comparator / control treatment
Identical placebo tablet, the same duration and mode of administration as the intervention

All participants will be prescribed oral folic acid at a minimum dose of 5 mg/week, 6 days/week
Control group
Placebo

Outcomes
Primary outcome [1] 302422 0
Reduction in hand pain score assessed using a 100mm Visual Analogue Scale
Timepoint [1] 302422 0
6 months after randomisation
Secondary outcome [1] 335939 0
Physical function assessed using Functional Index for Hand Osteoarthritis
Timepoint [1] 335939 0
3 and 6 months after randomisation
Secondary outcome [2] 335941 0
Quality of life assessed using Short Form-36
Timepoint [2] 335941 0
3 and 6 months after randomisation
Secondary outcome [3] 335942 0
Joint activity assessed using tender and swollen joint count
Timepoint [3] 335942 0
3 and 6 months after randomisation
Secondary outcome [4] 335943 0
Grip strength assessed using hand dynamometer
Timepoint [4] 335943 0
3 and 6 months after randomisation
Secondary outcome [5] 335944 0
Progression of synovitis assessed using magnetic resonance imaging of hand
Timepoint [5] 335944 0
6 months after randomisation or end of study
Secondary outcome [6] 335990 0
Progression of bone marrow lesions assessed using magnetic resonance imaging of hand
Timepoint [6] 335990 0
6 months after randomisation or end of study
Secondary outcome [7] 398667 0
Proportion of participants with radiographic progression of hand osteoarthritis assessed using hand x-ray
Timepoint [7] 398667 0
6 months after randomisation or end of study

Eligibility
Key inclusion criteria
1. Aged 40 - 75 years with symptomatic radiological hand osteoarthritis and synovitis
2. A pain score of greater than or equal to 40mm on a 100mm visual analogue scale and radiological osteoarthritis (Kellgren and Lawrence grade greater than or equal to 2) in at least one joint
3. Evidence of synovitis determined from magnetic resonance imaging with a grade greater than or equal to 1 in at least one joint
Minimum age
40 Years
Maximum age
75 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
1. Concomitant rheumatic disease, inflammatory joint disease, psoriatic arthritis, ankylosing spondylitis, or gout
2. Contraindication to methotrexate (e.g. renal, liver or haematological condition, cancer including skin cancer, serious infections requiring hospitalisation in the last 5 years, known or past infection with HIV, Hepatitis B or C, Tuberculosis, or known lung disease with scarring (any fibrosis or evidence of past tuberculosis exposure on chest x-ray), concurrent regular prednisolone use, taking regular Trimethoprim or Bactrim antibiotics, egg or flu vaccination allergy, women who are pregnant, breast-feeding or trying to become pregnant, or men who father a child)
3. Contraindication to magnetic resonance imaging (e.g. implanted pacemaker, metal sutures, presence of shrapnel or iron filings in the eye, or claustrophobia)
4. Unable to complete informed consent.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
numbered containers
central randomisation by computer
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Block randomization will be performed, stratified according to the study site. Randomisation will also utilise gender stratification.
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s

The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 3
Type of endpoint/s
Efficacy
Statistical methods / analysis
96 patients (allowing for a 20% dropout) will be sufficient (with 90% power) to detect the clinically significant differences between intervention and control groups in terms of a minimal clinically important difference in VAS pain of 15mm.
An intention-to-treat analysis, including all participants in their randomised groups regardless of their adherence to assigned treatments, will be performed in a blinded fashion. The effect of intervention on pain reduction and other pain and function outcomes measured at multiple time points will be analysed using mixed linear regression models, with a random intercept for participant. For measures only taken at baseline and a single follow-up time point, regression models will omit random intercepts and terms for time. Binary logistic regression will be used to assess the effect of intervention on structural progression at 6 months. The outcome of tender/swollen joint count will be analysed via a Poisson model fit via generalised estimating equations with an exchangeable working correlation structure to account for multiple measurements per participant. If more than 5% of participants are missing their primary outcome, multiple imputation will be applied to account for missing data. Sensitivity analyses will fit outcome regression models additionally adjusted for age, body mass index, and severity of radiographic OA and synovitis if baseline imbalances between randomised groups with respect to these variables are considered clinically important. A sensitivity analysis of the primary outcome will be undertaken to estimate the effect of methotrexate under the assumption of hypothetical complete compliance to treatment.

Recruitment
Recruitment status
Active, not recruiting
Date of first participant enrolment
Anticipated
1/09/2017
Actual
4/04/2018
Date of last participant enrolment
Anticipated
30/07/2021
Actual
8/11/2021
Date of last data collection
Anticipated
31/08/2022
Actual
Sample size
Target
96
Accrual to date
Final
97
Recruitment in Australia
Recruitment state(s)
SA,TAS,WA,VIC

Funding & Sponsors
Funding source category [1] 296724 0
Government body
Name [1] 296724 0
National Health and Medical Research Council
Country [1] 296724 0
Australia
Primary sponsor type
University
Name
Monash University
Address
School of Public Health and Preventive Medicine
Monash University
553 St Kilda Road
Melbourne, VIC 3004
Country
Australia
Secondary sponsor category [1] 295694 0
None
Name [1] 295694 0
Address [1] 295694 0
Country [1] 295694 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 297949 0
Alfred Hospital Ethics Committee
Ethics committee address [1] 297949 0
Ethics committee country [1] 297949 0
Australia
Date submitted for ethics approval [1] 297949 0
26/06/2017
Approval date [1] 297949 0
15/08/2017
Ethics approval number [1] 297949 0
290/17
Ethics committee name [2] 297950 0
Tasmania Health & Medical Human Research Ethics Committee
Ethics committee address [2] 297950 0
Ethics committee country [2] 297950 0
Australia
Date submitted for ethics approval [2] 297950 0
10/07/2017
Approval date [2] 297950 0
18/10/2017
Ethics approval number [2] 297950 0
H0016794
Ethics committee name [3] 297951 0
Central Adelaide Local Health Network Human Research Ethics Committee (CALHN HREC)
Ethics committee address [3] 297951 0
Ethics committee country [3] 297951 0
Australia
Date submitted for ethics approval [3] 297951 0
10/07/2017
Approval date [3] 297951 0
09/10/2018
Ethics approval number [3] 297951 0
HREC/18/CALHN/458
Ethics committee name [4] 297952 0
South Metropolitan Health Service Human Research Ethics Committee
Ethics committee address [4] 297952 0
Ethics committee country [4] 297952 0
Australia
Date submitted for ethics approval [4] 297952 0
10/07/2017
Approval date [4] 297952 0
12/01/2018
Ethics approval number [4] 297952 0
RGS0000000573

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 75554 0
Prof Flavia Cicuttini
Address 75554 0
School of Public Health and Preventive Medicine
Monash University
553 St Kilda Road
Melbourne, VIC 3004
Country 75554 0
Australia
Phone 75554 0
+ 61 3 9903 0158
Fax 75554 0
+ 61 3 9903 0556
Email 75554 0
[email protected]
Contact person for public queries
Name 75555 0
Flavia Cicuttini
Address 75555 0
School of Public Health and Preventive Medicine
Monash University
553 St Kilda Road
Melbourne, VIC 3004
Country 75555 0
Australia
Phone 75555 0
+ 61 3 9903 0158
Fax 75555 0
+ 61 3 9903 0556
Email 75555 0
[email protected]
Contact person for scientific queries
Name 75556 0
Flavia Cicuttini
Address 75556 0
School of Public Health and Preventive Medicine
Monash University
553 St Kilda Road
Melbourne, VIC 3004
Country 75556 0
Australia
Phone 75556 0
+ 61 3 9903 0158
Fax 75556 0
+ 61 3 9903 0556
Email 75556 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment
The IPD will be kept confidential. Access to computer or paper-based records with identifiable data is restricted to authorised staff.


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
SourceTitleYear of PublicationDOI
EmbaseMETHODS - A randomised controlled trial of METhotrexate to treat Hand Osteoarthritis with Synovitis: study protocol for a randomised controlled trial.2021https://dx.doi.org/10.1186/s12891-021-04842-0
EmbaseMethotrexate to treat hand osteoarthritis with synovitis (METHODS): an Australian, multisite, parallel-group, double-blind, randomised, placebo-controlled trial.2023https://dx.doi.org/10.1016/S0140-6736%2823%2901572-6
N.B. These documents automatically identified may not have been verified by the study sponsor.