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Clinical Trial Details

Trial ID: L0743
Source ID: NCT02424851
Associated Drug: Bortezomib
Title: Optimising Renal Outcome in Myeloma Renal Failure
Acronym: OPTIMAL
Status: COMPLETED
Study Results: YES
Results: https://ClinicalTrials.gov/show/NCT02424851/results
Conditions: Multiple Myeloma|Chronic Kidney Disease
Interventions: DRUG: Bortezomib|DRUG: Thalidomide|DRUG: Bendamustine|DRUG: Dexamethasone
Outcome Measures: Primary: Number of Participants With >50% Reduction From Baseline in Serum Free Light Chain, End of week 6 (after receiving two cycles of therapy)|Number of Participants With Different Renal Responses to Treatment, End of week 12 (after receiving 4 cycles of therapy) | Secondary: Haematological and Non-haematological Toxicity in Both Treatment Arms, End of weeks 3, 6, 9, 12 (after receiving 4 cycles of therapy), 30 days after final treatment and 12 months after randomisation|Overall Survival, 1 month post end of treatment and 1 year post randomisation|Renal Response After Two Cycles of Trial Treatment, End of 2nd treatment cycle, week 6|Quality of Life Measured by the EQ-5D-3L Questionnaire at Baseline and 1 Month Follow up, The EQ-5D-3L descriptive system comprises the following five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension is scored on a scale of 1 to 3: 1 (no problems), 2 (some problems), and 3 (extreme problems). Higher score equates to a worse outcome. As stated in the official EQ-5D user guide, patient responses to the 5 questions were converted into a single index value as per Dolan P (1997). Modeling valuations for EuroQol health states. Med Care 35(11):1095-108. These index values, with country specific value sets, facilitate the calculation of quality-adjusted life years (QALYs) that are used to inform economic evaluations of health care interventions. In the UK, the values range from -0.594 to +1., Baseline and 1 month follow up
Sponsor/Collaborators: Sponsor: Oxford University Hospitals NHS Trust | Collaborators: Janssen-Cilag Ltd.|Bloodwise|University of Warwick|University of Birmingham
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE2
Enrollment: 31
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: TREATMENT
Start Date: 2014-11
Completion Date: 2020-04-20
Results First Posted: 2022-01-27
Last Update Posted: 2022-01-27
Locations: Basingstoke & North Hampshire Hospital, Basingstoke, United Kingdom|Heartlands Hospitals, Birmingham, United Kingdom|Kent & Canterbury Hospital, Canterbury, CT1 3NG, United Kingdom|St Helier Hospital, Epsom, United Kingdom|Royal Liverpool Hospital, Liverpool, United Kingdom|Kings College Hospital, London, United Kingdom|Churchill Hospital, Oxford, OX3 7LE, United Kingdom|Queen Alexandra Hospital, Portsmouth, United Kingdom|Great Western Hospital, Swindon, United Kingdom
URL: https://clinicaltrials.gov/show/NCT02424851