Cardiovascular Diseases Clinical Trial
Official title:
Trial of Statin Holiday in Patients Receiving Maintenance Dialysis
NCT number | NCT03663049 |
Other study ID # | 210890 |
Secondary ID | |
Status | Recruiting |
Phase | Phase 4 |
First received | |
Last updated | |
Start date | August 17, 2018 |
Est. completion date | May 2021 |
Patients who are on chronic dialysis and 70 and older are frequently on multiple medications including statins. However, the benefit of statins in dialysis patient population is uncertain. Several randomized trials showed no benefit of statins on mortality in dialysis patient population. Guidelines recommend not starting statins in patients on dialysis who are not already taking them. However, there are no guidelines on what to do in patients who are already taking statins. The investigators are doing a short pilot study to discontinue statin in our dialysis patient population and evaluating the effects on discontinuation of statins on quality of life, cognition, as physical strength.
Status | Recruiting |
Enrollment | 30 |
Est. completion date | May 2021 |
Est. primary completion date | May 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 70 Years and older |
Eligibility |
Inclusion Criteria: 1. Age 70 years and older, 2. Receiving maintenance dialysis for at least 6 months, 3. Must be on a statin medication, 4. Receiving dialysis at the Loyola University Medical Center dialysis unit , 5. Can be on hemodialysis or peritoneal dialysis, Exclusion Criteria: 1. Age less than 70 years old 2. Any recent hospital admission (within 2 weeks) 3. Recent dialysis start (within 6 months) 4. Any cancer diagnosis, with exception of innocuous skin cancers and previously treated cancers 5. Any recent (< 1 year) solid organ transplant 6. Active on kidney transplant wait list 7. Recent acute coronary event (e.g. recent NSTEMI, stent, angioplasty, CABG) within 6 months 8. Non-English speaking 9. Diagnosis of dementia 10. Patients who are unable to provide informed consent |
Country | Name | City | State |
---|---|---|---|
United States | Loyola University Medical Center | Maywood | Illinois |
Lead Sponsor | Collaborator |
---|---|
Loyola University |
United States,
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* Note: There are 20 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Change in cognition | Cognition will be measured with trail making test at baseline and again at 6 and 12 weeks | Change in cognition over 12 weeks | |
Other | Change in frailty | Frailty will be measured with the Fatigue, Resistance, Aeorbic, Illnesses, and Loss of weight (FRAIL) questionnaire at baseline and again at 6 and 12 weeks. The questionnaire rates each of the five items as 0 for no and 1 for yes, with a total score of 5 possible. Scoring scale: 1-2= pre-frail; 3 or greater=frailty | Change in frailty at 12 weeks | |
Other | Change in mobility | Fall risk will be measured with the Get up and go test at baseline and again at 6 and 12 weeks. Time interpretation scale: 10 seconds or less=normal; 20 seconds or less= good mobility; 20 seconds or more = mobility problems, need for a mobility aid | Change in mobility at 12 weeks | |
Primary | Change in quality of life | Change in quality of life will be measured by the Short Form Survey 20 (SF-20). The survey assesses quality of life via 20 questions across 6 domains: physical functioning (6 questions), role functioning (2 questions), social functioning (1 question), mental health (5 questions), health perceptions (5 questions), and pain (1 question). Scores across each of these domains are reported on a 0% to 100% scale, with 0% representing the worst possible score in that domain and 100% the best possible score. | Change in quality of life over 12 weeks | |
Secondary | Change in handgrip strength | Handgrip strength will be measured at baseline and again at 6 and 12 weeks | Change in handgrip strength over 12 weeks |
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