Systemic Sclerosis
Conditions
Keywords
Diffuse cutaneous systemic sclerosis (dcSSc), Prednisolone, Randomised Controlled Trial, Disability, Pain, Fatigue
Brief summary
This is a randomised placebo-controlled study of moderate dose prednisolone for 6 months in patients with early diffuse cutaneous systemic sclerosis (dcSSc). Seventy-two patients within 3 years of the onset of skin thickening will be recruited from 14 UK centres over 3 years. Co-primary end-points will be the Health Assessment Questionnaire Disability Index (HAQ-DI) and the modified Rodnan skin score (mRSS). Patients will be assessed 5 times: screening, baseline, 6 weeks, 3 and 6 months, with a code-break on exit from the study at 6 months. Please note: From August 2020, the trial was re-started following halt due to Covid-19 as open-label. The placebo arm is the 'no treatment' arm and there is no longer a code-break at study exit.
Detailed description
The study is a non-commercial phase II randomised, double-blind, placebo-controlled, multi-centre study to test moderate dose prednisolone versus placebo in patients with early diffuse cutaneous systemic sclerosis (dcSSc). Our aim is to investigate whether treatment with the steroid prednisolone is beneficial in patients with early diffuse cutaneous systemic sclerosis (also termed scleroderma). This is a controversial subject. Although it is very possible that prednisolone can help relieve the severe pain, itching, and disability (due to contractures and musculoskeletal involvement) of early diffuse scleroderma, doctors are often reluctant to prescribe prednisolone because of possible side effects, particularly an increased risk of serious kidney problems. Our proposed trial, treating patients with either prednisolone or placebo therapy for 6 months, should provide clinicians with a long awaited answer to the important clinical question: Can prednisolone be used as a therapy in this group of patients? The study, funded by Arthritis Research UK, aims to determine: 1. Is moderate dose prednisolone effective in reducing pain, disability and skin thickening in patients with early diffuse scleroderma? 2. Is moderate dose prednisolone a safe therapy in patients with early diffuse scleroderma (with particular reference to kidney function)? If the answer to both is 'yes', then prednisolone therapy will be much more widely prescribed for this patient group. The patient population will be selected from individuals with early dcSSc, as defined by skin involvement of less than 3 years, who are considered potentially able to benefit from this treatment. Following screening, to minimise bias, eligible patients will be randomised at the baseline visit to receive either daily moderate dose prednisolone (as determined by body weight) or a matched placebo. To further eliminate subjective and unrecognised bias both the research team and patients will be blind to the randomisation. A placebo control, as opposed to an active treatment control, will be administered. This is necessary as the study treatment is adjunctive to and not a substitute for any other therapies which may be prescribed, such as immunosuppressant therapies. Patients will attend on 5 occasions (screen, baseline, 6 weeks, 3 and 6 months). All patients will be considered off-study at the end of the 6 month visit whereupon the treatment code will be broken. At each visit a number of measurements will be taken including functional ability, degree of skin involvement (skin score), mood and kidney function. This will allow us to determine whether 'active' (prednisolone) therapy is effective and free from serious side-effects. Please note: from August 2020, due to Covid-19 the trial was re-designed and re-started following trial halt as open-label. A placebo is no longer required. The aims, primary outcome measures and number of visits remain unchanged. However, to further mitigate the ongoing impact of Covid-19, the screen and baseline assessments may now be conducted at the same visit. Remote visits can also be carried out at 6 weeks and 6 months, if necessary.
Interventions
5mg prednisolone, once a day for 6 months
DRUGPlacebo oral capsule; From August 2020 'no additional treatment'
Matched placebo capsule, once a day for 6 months; From August 2020 - no additional treatment above standard of care medication
Sponsors
Versus Arthritis
Prof. Ariane herrick
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)
Masking description
Double-blind. The trial management team are blind to treatment allocation for the duration of the trial. The site research teams and patients are blind to treatment until code-break. At this point the on-site team and patient are unblind to allocation for continuing care. The site pharmacy personnel, PRedSS trial monitor and supervising statistician are unblind throughout. From August 2020: Open-Label - The patient, site research team and site pharmacy are unblind. The trial management team are unblind for patients recruited from August 2020 onwards but remain blind to patients randomised to trial under the double-blind design. The trial monitor and trial statistician continue to be unblind for all patients randomised to trial.
Intervention model description
Patients are allocated to received either prednisolone or matched placebo for the duration of the trial. The allocation is randomised 1:1. From August 2020: Under the open-label design, patients are allocated to receive prednisolone or no additional treatment. The randomisation allocation is 1:1.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Patients presenting with dcSSc with skin involvement extending to the proximal limb and/or trunk. 2. Male or female age ≥ 18 years. 3. Skin involvement of less than 3 years defined by patient report or clinician opinion. 4. Patient is able and willing to follow the requirements of the study. 5. Fully written informed consent.
Exclusion criteria
1. Patients with significant uncontrolled Stage 1 Hypertension (clinic BP \>140/90mmHg i.e. either \>140mmHg OR \>90mmHg). Patients with previous hypertension which is controlled (clinic BP \<140/90mmHg) for at least 4 weeks are considered eligible. 2. Previous renal crisis or significant renal impairment (estimated Glomerular Filtration Rate (eGFR) \< 40 ml/min). 3. Patients currently on steroid therapy, or previous steroid therapy within the last 4 weeks, with the exception of inhaled steroids for respiratory diseases. 4. Patients currently participating in another randomised controlled trial of an investigational agent or device, or previous participation within the last 30 days. 5. Patients currently receiving an immunosuppressant or biologic therapy the dose of which has changed in the last 4 weeks prior to the baseline visit, or is likely to change during the first 3 months of study treatment. 6. Patients with major myositis or inflammatory arthritis. Patients with low level myositis or inflammatory arthritis are eligible for inclusion (for example, in the case of myositis, a creatine kinase less than 4 times the upper limit of normal or myositis only demonstrable on magnetic resonance imaging). 7. Female patients who are pregnant at time of screening. 8. Female patients who are breastfeeding. 9. Patients with significant inflammatory bowel disease as judged by the investigator. 10. It is important that patients do not suddenly stop taking the study medication. Patients who do not fully understand this, will be excluded. 11. Patients who are unwilling or unable to provide informed consent.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| modified Rodnan Skin Score (mRSS) | Baseline to 3 months | The difference in mRSS at 3 months |
| Health Assessment Questionnaire Disability Index (HAQ-DI) | Baseline to 3 months | The mean difference in HAQ-DI at 3 months |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Functional ability - Assessed by Questionnaire | Baseline to 6 weeks, 3 months and 6 months | 11-point Scleroderma Functional Index |
| Pain associated with itch - Assessed by Questionnaire | Baseline to 6 weeks, 3 months and 6 months | Assessment of Pruritus |
| Hand function - Assessed by Questionnaire | Baseline to 6 weeks, 3 months and 6 months | Cochin Hand Function |
| Fatigue - Assessed by Questionnaire | Baseline to 6 weeks, 3 months and 6 months | Functional Assessment of Chronic Illness Therapy (FACIT) |
| Quality of life and functional ability - Assessed by Questionnaire | Baseline to 6 weeks and 6 months | HAQ-DI |
| Health related quality of life - Assessed by Questionnaire | Baseline to 6 weeks, 3 months and 6 months | Helplessness Questionnaire |
| Health related quality of Life - Assessed by Questionnaire | Baseline to 6 weeks, 3 months and 6 months | EuroQol 5 Dimensions |
| Assessment of pain - Clinician assessment | Baseline to 6 weeks, 3 months and 6 months | Digital Ulcer Count: The site and total number of ulcers on the hand are recorded by the patients clinician on a diagram of a hand |
| Pain and disability - Assessed by Questionnaire | Baseline to 6 weeks, 3 months and 6 months | Assessment of Arthritis Index |
| Anxiety and depression - Assessed by questionnaire | Baseline to 6 weeks, 3 months and 6 months | Hospital Anxiety and Depression Scale (HADS) . This questionnaire has 14 questions, each with 4 options designed to assess aspects of mental health |
| Pain and disability | Baseline to 6 weeks and 6 months | Skin involvement as measured by the mRSS |
Countries
United Kingdom
Outcome results
None listed