Thalidomide for the Treatment of Malnutrition Inflammation Syndrome in Peritoneal Dialysis Patients
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Purpose
Hypothesis In peritoneal dialysis (PD) patients, malnutrition, inflammation and atherosclerotic cardiovascular disease commonly coexist. The triad has been coined the “MIA syndrome”. Proinflammatory cytokines, such as tumor necrosis factor-alpha (TNF-), plays a central role in the pathogenesis of the MIA syndrome. Thalidomide selectively inhibits the production of TNF- and represents a valuable anti-cytokine therapy.
Specific Aim To study the effect of thalidomide in attenuating or reversing malnutrition and systemic inflammation in PD patients.
Research Plan
- Design: Double-blinded randomised prospective placebo control trial.
- Setting: Renal unit of a university teaching hospital.
- Subjects: Sixty prevalent PD patients with evidence of malnutrition.
- Interventions: Patients will be randomised to receive either oral thalidomide 100 mg nocte or placebo.
- Main outcome measures: Patients will be followed for 1 year. Nutritional parameters including serum albumin, subjective global assessment, malnutrition-inflammation score, normalised protein nitrogen appearance, fat-free edema-free body mass and anthropometry measurements will be monitored. Systemic inflammatory markers such as serum C-reactive protein and IL-6 will be assayed. Hospitalisation, cardiovascular events, and overall patient survival will also be compared during study period.
Expected Outcome
Nutritional parameters and markers of systemic inflammation are expected to improve with thalidomide therapy. The magnitude of improvement in nutrition, as well as patient morbidity, will be compared with placebo.
In Hong Kong, 80% of end-stage renal failure patients are treated with PD. Malnutrition, cardiovascular disease and systemic inflammatory response are all common in our clinical practice. They are major causes of patient morbidity and mortality. As a readily available anti-cytokine therapy, thalidomide may represent a valuable treatment of the MIA syndrome. The proposed study will provide important insight on the clinical benefit of thalidomide treatment in malnourished PD patients, which accounts for about one-third of our dialysis population.
| Condition | Intervention | Phase |
|---|---|---|
|
Peritoneal Dialysis Malnutrition |
Drug: thalidomide |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double-Blind Primary Purpose: Treatment |
| Official Title: | Thalidomide for the Treatment of Malnutrition Inflammation Syndrome in Peritoneal Dialysis Patients: A Randomized Control Trial |
- Nutritional status
- Change in arterial pulse wave velocity
- Total number of days of hospital admission during study period
- Composite cardiovascular end point
| Estimated Enrollment: | 60 |
| Study Start Date: | January 2007 |
| Estimated Study Completion Date: | December 2008 |
Show Detailed Description
Eligibility| Ages Eligible for Study: | 18 Years to 80 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- clinically stable adult patients (18 to 80 years old) on PD; and
evidence of malnutrition:
- overall subjective global assessment score 5; or
- malnutrition inflammation score 9; or
- serum albumin 35 g/L
- written patient informed consent
Exclusion Criteria:
- Patients who are planned to have elective living donor transplant within 6 months
- Patients who are planned to transfer to other renal center within 6 months
- High likelihood of early withdrawal from the study (e.g. myocardial infarction, severe or unstable coronary disease, stroke, severe liver disease within 3 months)
- Active infection or systemic inflammatory disease.
- Current malignant disease
- Pregnancy or breast-feeding
- Women of childbearing potential with unreliable birth control methods
- Known hypersensitivity to thalidomide
Contacts and Locations| Hong Kong | |
| Renal Unit, Department of Medicine & Therapeutics, Prince of Wales Hospital | |
| Hong Kong, Hong Kong | |
| Principal Investigator: | Cheuk-Chun Szeto, MD | Chinese University of Hong Kong |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00390247 History of Changes |
| Other Study ID Numbers: | CRE-2006.291 |
| Study First Received: | October 18, 2006 |
| Last Updated: | April 5, 2007 |
| Health Authority: | Hong Kong: Joint CUHK-NTEC Clinical Research Ethics Committee |
Additional relevant MeSH terms:
|
Inflammation Malnutrition Pathologic Processes Nutrition Disorders Thalidomide Immunosuppressive Agents Immunologic Factors Physiological Effects of Drugs Pharmacologic Actions |
Leprostatic Agents Anti-Bacterial Agents Anti-Infective Agents Therapeutic Uses Angiogenesis Inhibitors Angiogenesis Modulating Agents Growth Substances Growth Inhibitors Antineoplastic Agents |
ClinicalTrials.gov processed this record on May 16, 2013