Study of treatments for pyoderma gangrenosum
| ISRCTN | ISRCTN35898459 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN35898459 |
| Clinical Trials Information System (CTIS) | 2008-008291-14 |
| Protocol serial number | UKDCTN0901 |
| Sponsor | Nottingham University Hospitals NHS Trust (UK) |
| Funder | National Institute for Health Research (NIHR) (UK) - Programme Grant for Applied Research (PGfAR) (ref: RP-PG-0407-10177): awarded to the Centre of Evidence Based Dermatology at the University of Nottingham |
- Submission date
- 02/04/2009
- Registration date
- 26/05/2009
- Last edited
- 06/02/2017
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Skin and Connective Tissue Diseases
Plain English summary of protocol
Background and study aims
Pyoderma gangrenosum is a rare skin disease. It causes painful, rapidly spreading ulcers on the skin, and can take many months to heal. Although there are different medications available to treat pyoderma gangrenosum, there is no information on which of these is best to use. The two most commonly prescribed tablet (oral) medications for pyoderma gangrenosum are ciclosporin and prednisolone. This study compares these treatments head-to-head to find out whether one works better than the other, and the likely side effects of treatment.
Who can participate?
Patients aged 18 or over who have been diagnosed with pyoderma gangrenosum and have a measurable ulceration (e.g. not pustular pyoderma gangrenosum).
What does the study involve?
Participants are randomly allocated to receive either oral prednisolone or oral ciclosporin. Scheduled clinic visits take place at week 0, week 2, week 6 and after 6 months of treatment (or sooner if the ulcer has healed). Ulcer healing is assessed using digital images of the ulcer by a clinician unaware of the treatment allocation.
What are the possible benefits and risks of participating?
Both ciclosporin and prednisolone cause side effects in some people. It is not known whether one medication will be better (more effective) than the other, as that is what our study is looking at.
Where is the study run from?
The trial is being managed through the Nottingham Clinical Trials Unit at the University of Nottingham (UK).
When is the study starting and how long is it expected to run for?
Recruitment is taking place over a four-year period, starting April 2009, in approximately 50 hospitals across the UK.
Who is funding the study?
National Institute for Health Research (NIHR) (UK)
Who is the main contact?
Prof. Hywel Williams
hywel.williams@nottingham.ac.uk
Contact information
Scientific
University of Nottingham
Centre of Evidence Based Dermatology
King's Meadow Campus
Lenton Lane
Nottingham
NG7 2NR
United Kingdom
 ORCID ID |
0000-0002-5646-3093 |
|---|---|
| Phone | +44 (0)115 8230489 |
| hywel.williams@nottingham.ac.uk |
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Multicentre parallel-group single-blind randomised controlled trial with a parallel observational study |
| Secondary study design | Randomised parallel trial |
| Study type | Participant information sheet |
| Scientific title | Randomised controlled trial of treatments for pyoderma gangrensoum |
| Study acronym | STOP GAP |
| Study objectives | Pyoderma gangrenosum (PG) is a mutilating, very painful skin disease that often affects people with an underlying internal disease (such as inflammatory bowel disease, monoclonal gammopathy and rheumatoid arthritis). It starts as a reddish purple bump in the skin that develops into a large, deep, spreading ulcer in a matter of days. People with PG are often misdiagnosed, and spend a long time in hospital waiting for the affected areas to heal (ulcers can last for a variable time on average healing after 3 - 4 months). Patients are not able to work, require daily dressings, have a high need for health care resources, and have very poor quality of life. Patients often have repeat episodes of PG and may have multiple lesions. Treatment of PG usually involves immunosuppression or immunomodulation. The purpose of this trial is to evaluate the efficacy and safety of the two most commonly used systemic treatments for pyoderma gangrenosum (PG). The study aims to test the hypothesis that systemic ciclosporin (4 mg/kg/day) is more effective than systemic prednisolone (0.75 mg/kg/day) for oral therapy of PG. The hypothesis is that ciclosporin gains control of PG more rapidly, and reduces the time to healing for patients with PG compared to treatment with oral prednisolone. |
| Ethics approval(s) | The Northern and Yorkshire Research Ethics Committee, 15/02/2009, ref: 09/H0903/5 |
| Health condition(s) or problem(s) studied | Pyoderma gangrenosum (PG) |
| Intervention | Patients entered into the RCT will be randomised to prednisolone (0.75 mg/kg/day) or ciclosporin (4 mg/kg/day), up to a ceiling dose of 75 mg/day prednisolone and 400 mg/day ciclosporin. Patients entered into the observational study will be prescribed topical therapy. Participants will be treated for up to 6 months during the trial and followed up until the end of the trial. |
| Intervention type | Drug |
| Phase | Phase IV |
| Drug / device / biological / vaccine name(s) | Ciclosporin, prednisolone |
| Primary outcome measure(s) |
Velocity of healing at 6 weeks. This will be captured for a single target lesion per patient and measured using digital photography and vascular endothelial volume (VEV) computerised planimetry. If multiple lesions are present, the target lesion should be the lesion that is most able to be photographed on a single plane (i.e., not around the curvature of a limb) for study will be the largest of those present. Digital images will be taken at baseline, 6 weeks and when the ulcer has healed (maximum of 6 months). In addition, maximum longitudinal length and maximum perpendicular width will be measured in order to provide some measure of improvement in case of difficulties with the digital images. This will be converted to approximate area by the formula: length x width x 0.785, which approximates to an ellipse for the purpose of randomisation and analysis. |
| Key secondary outcome measure(s) |
1. Time to healing - assessed by participants (estimated to the nearest week) based on the time at which sterile dressings are no longer required for the wound. Healing will be confirmed using digital photography at the first opportunity. Information will be provided to participants with instructions on how to report healing of the ulcer. Lesions that remain unhealed after 6 months will be considered to be treatment failures. Time to healing is a more clinically relevant outcome than velocity of healing. It also gives some indication of duration of treatment, which therefore gives an indication of cumulative drug toxicity. |
| Completion date | 31/08/2013 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Adult |
| Lower age limit | 18 Years |
| Sex | All |
| Target sample size at registration | 140 |
| Key inclusion criteria | 1. PG as diagnosed by the recruiting dermatologist. An ulcerative lesion may have mixed aetiology, but provided the investigator has confidence that a clinical diagnosis of PG is appropriate then they are eligible. Other contributing factors and atypical features will be captured in the case report form. 2. Must have a measurable ulceration (e.g., not pustular pyoderma gangrenosum) 3. Age over 18 years, either sex 4. Able to provide written, informed consent |
| Key exclusion criteria | Patients cannot participate in either arms of the trial if they have any of the following: 1. Granulomatous PG - this condition is very rare and may respond differently to treatment 2. Concomitant ciclosporin, prednisolone or intravenous immunoglobulin (IVIG) therapy in the previous month 3. Already participating in another clinical trial Exclusions for the randomised controlled trial only are as follows: 4. Pregnant, lactating or at risk of pregnancy 5. Hypersensitivity to prednisolone or ciclosporin 6. Biopsy not consistent with PG 7. Clinically significant renal impairment that would result in the investigator not normally treating with either study drug 8. Any pre-treatment investigations, the results of which would prompt the investigator not to use either study drug 9. A diagnosis of malignancy or pre-malignant disease where treatments might interfere with ongoing therapy or might cause harm (e.g., history of lymphoma, cervical epithelial neoplasia [CIN], systemic cytotoxic therapy) 10. The patient has a concurrent medical condition that means the investigator would not normally treat the patient with either of the study drugs (for example: a degree of hypertension that would not lead to using either of the study drugs, advanced heart failure, poorly-controlled diabetes, history of peptic ulcer, malignancy in previous years) 11. Administration of a live vaccine (bacillus calmette-guerin [BCG], measles, mumps, rubella, yellow fever, oral polio, oral typhoid) within the last 2 weeks |
| Date of first enrolment | 08/06/2009 |
| Date of final enrolment | 31/08/2013 |
Locations
Countries of recruitment
- United Kingdom
- England
Study participating centres
NG7 2NR
United Kingdom
United Kingdom
Results and Publications
| Individual participant data (IPD) Intention to share | Yes |
|---|---|
| IPD sharing plan summary | Available on request |
| IPD sharing plan |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Results article | results | 12/06/2015 | Yes | No | |
| Results article | results | 02/02/2017 | Yes | No | |
| Protocol article | protocol | 28/04/2012 | Yes | No | |
| HRA research summary | 28/06/2023 | No | No | ||
| Participant information sheet | Participant information sheet | 11/11/2025 | 11/11/2025 | No | Yes |
| Study website | Study website | 11/11/2025 | 11/11/2025 | No | Yes |
Editorial Notes
06/02/2017: Publication reference added.
