Multiple Myeloma Clinical Trial
— MELODYOfficial title:
Multiple Myeloma Spinal Disease Study; A Multi-centre, Prospective, Single Blinded, Randomized, Controlled Study to Compare Conservative Management Alone Vs. Balloon Kyphoplasty With the Treatment of VCFs in Patients With Multiple Myeloma
Verified date | April 2018 |
Source | Royal National Orthopaedic Hospital NHS Trust |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to determine whether surgical treatment, balloon kyphoplasty is
more effective compared to conservative treatment alone (sham procedure) when assessing
clinical, translational, radiological & patient outcomes in patients with multiple myeloma.
Subjects will be recruited to the study if they have VAS score ≥ 6 and has given informed
consent to participate in the Melody Study will be randomised to Arm 1 Sham Procedure and
Conservative treatment or Arm 2 Balloon Kyphoplasty and Conservative treatment. Subjects
recruited to Arm 1 (Sham Procedure and Conservative treatment) can cross over into Arm 2
(Balloon Kyphoplasty and Conservative Treatment) if they have a VAS score ≥ 6 between 8-12
weeks.
Status | Terminated |
Enrollment | 2 |
Est. completion date | March 28, 2018 |
Est. primary completion date | March 28, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility |
Inclusion Criteria: - Age = 18 and =80 years old - Diagnosis of Multiple Myeloma - Confirmed acute (MRI, a detectable low signal T1 ± oedema) painful vertebral compression fracture(s) VAS score is =6 - The patient is able to read and understand the Patient Information Sheet and study procedures - The patient is able and willing to give written informed consent Exclusion Criteria: - Contraindications to anaesthesia - Cord Compression or large epidural mass necessitating conservative management before balloon kyphoplasty - Pain unrelated to vertebral collapse - Infection at the site - Presence of overt instability as judged by the principle investigator - Known pregnancy at time of screening - Severe Cardiopulmonary insufficiency - Osteoblastic lesions - Any co-morbidity, (e.g., diabetes, heart condition, obesity, psychiatric illness) which, in the opinion of the investigator, is of a severe enough nature to; interfere with the patient's ability to complete the study assessments; or present an unacceptable risk to the patient's safety to undergo study treatment |
Country | Name | City | State |
---|---|---|---|
United Kingdom | Royal National Orthopaedic NHS Trust, Brockley Hill | Stanmore | UK |
Lead Sponsor | Collaborator |
---|---|
Royal National Orthopaedic Hospital NHS Trust |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | the effect of sham procedure & conservative management alone (arm 1) versus balloon kyphoplasty (arm 2) on patient reported pain scores as assessed by VAS (at week 4) | At week 4 | ||
Secondary | the effect of conservative management alone versus balloon kyphoplasty on patient reported pain scores as assessed by VAS (at weeks 1, 8, 12, 16, 26, year 1 and year 2) | At week 1, 8, 12, 26, year 1 and year 2 | ||
Secondary | the pain relief requirements of conservative management alone versus balloon kyphoplasty using a daily pain diary (capturing usage of pain relief by type) | At week 1, 8, 12, 26, year 1 and year 2 | ||
Secondary | the effect of conservative management alone versus balloon kyphoplasty on patient reported Quality Of Life outcomes | At week 1, 8, 12, 26, year 1 and year 2 | ||
Secondary | procedure related complications of conservative management alone versus balloon kyphoplasty | recording of any adverse events | At week 1, 8, 12, 26, year 1 and year 2 | |
Secondary | the cost utility of the conservative management alone versus the balloon kyphoplasty | Data collected for all intervention groups from the study will be assessed to compare the overall cost of care for conservative management vs. kyphoplasty | at 2 years |
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