The study aimed to pilot the viability of a full scale randomised comparison of 2 steroid doses in malignant spinal cord compression, to establish safety of high dose dexamethasone in this setting in Australia, to test web registration and randomisation and to compare different functional outcome measures.
Malignant spinal cord compression (MSCC) is an uncommon condition with an estimated annual incidence of 2.5 per 100,000. It is a dreaded complication of malignancy because of the severe impact paralysis and sphincter disturbance has on quality and duration of survival. Rat models have demonstrated the effectiveness of high doses of steroids. Only three randomised controlled trials (RCTs) have been published. The first compared radiotherapy to laminectomy plus radiotherapy in a series of 29 patients and failed to show any significant differences The widespread commonly used dose of Dexamethasone in Australia at that time was 16 mg/24 hr and the main concern for implementing higher doses was the toxicity profile reported in the few small randomised comparisons available at the time.In view of the conflict between standard Australian practice versus published (overseas) guidelines, a randomised comparison was proposed in Australia. This study was a pilot study initiated to determine the viability of a large trial, to pilot the use of web technology for trial conduct and to determine clinically useful outcome measures apart from simple ambulation rates. Comparisons: Patients randomised to receive either 16mg/24hr or 96mg/24hr dexamethasone.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
20
St George Hospital
Kogarah, New South Wales, Australia
Satisfactory recruitment
Time frame: Failure to accrue 30 patients in 15 months will initiate early closure of this study.
Acceptable steroid toxicity rate at 28 days with reference to baseline.
Time frame: 28 days
Ambulation rates at 1 month
Time frame: 1 month
Barthel Index
Time frame: Final analysis when all patients have been followed for 1 month
Functional Independence (FIM)
Time frame: Final analysis when all patients have been followed for 1 month
Functional Improvement Score (FIS)within 2 weeks with reference to baseline
Time frame: 2 weeks
Pain
Time frame: Final analysis when all patients have been followed for 1 month
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