Diabetes Mellitus, Type 2 Clinical Trial
Official title:
Continuous Glycemia Monitoring in Perioperative Period in Patients Undergoing Total Knee or Hip Arthroplasty: a Protocol of Observational Study
All across surgery specialties, wound or implant infections constitute rare, yet potentially severe complications of surgical procedure. It is considered, that glucose metabolism disorders, e.g. diabetes, are one of the main risk factors of such condition. Aim of the study The aim of the study is a prospective evaluation of glucose blood level and its variability during 2 weeks before hospitalization and 2 weeks of postoperative period in patients, that will undergo elective orthopaedic surgeries, and its impact on number of cardiovascular and orthopaedic complications. Materials and methods To this study, patients qualified for elective total knee or hip replacement in the single orthopedic center will be recruited. 100 patients will be included in this study. Every patient will be evaluated on the risk of developing diabetes mellitus in 10 years time and on the risk of death in 10 years due to the cardiovascular events. 14 days before procedure patients will have continuous glucose level measurement sensor implemented in subcutaneous tissue. After 14 days, during standard visit for stitches removal, the sensor will be removed and glycemia data will be collected. Next, patients will have their casual glucose blood level checked and surgery outcome, cardiovascular events or surgery complication risk evaluated in 3-, 6- and 12 month follow-up visits. Expected benefits of the study Results of this study may allow to define impact of orthopaedic treatment on glycemia and possible necessity to modify treatment of hyperglycemia in perioperative period in patients with Diabetes Mellitus type 2 (DM2). Moreover it will allow to specify change of glucose levels and possibly implicating a need to monitor perioperative glycemia in patients without carbohydrate metabolism disorders. Additionally, the study will help to evaluate corelation between perioperative glucose blood level and the risk of cardiovascular events or surgical complications in 1-year after the procedure, which may decrease the risk of such incidents in the future (e.g. by adequate control and effective treatment of hyperglycemia), hence may result in reduction of mortality and lesser lowering of the quality of life in patients with DM2 or high risk of it.
Status | Not yet recruiting |
Enrollment | 100 |
Est. completion date | December 2022 |
Est. primary completion date | May 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility | Inclusion Criteria: - Patients hospitalized in the Department of Orthopedics and Rehabilitation of Medical University of Warsaw - Willingness to participate in the study - Qualified for total knee or hip replacement due to the primary osteoarthritis - Age above 18 years Exclusion Criteria: - No acceptance to participate in the study - Qualified for non-surgical treatment - Patients with other diseases but diabetes mellitus, compensated thyroid disorders and hypertension - Patients with poorly-controled diabetes mellitus and/or poorly-controlled hypertension - Patients with diabetes type 1 - Patients from the rest-home - Patients who had previous lower limb surgeries - Patients who in opinion of research team might be poorly compliant - Patients during pregnancy - Patients who are not fluent in polish language |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Medical University of Warsaw |
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* Note: There are 27 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes of glycemia levels during perioperative period | Continuous glycemia level monitoring with use of subcutaneously implanted device | 4 weeks (14 days preoperatively and 14 postoperatively) | |
Primary | Rate and type cardiovascular events during follow-up | Any cardiovascular events during follow-up (heart stroke, brain stroke, coronal arteries disease, transient ischaemic attack (TIA) | 12-months postoperatively | |
Primary | Rate and type of complications | Any surgical site and/or implants complications during follow-up | 12-months postoperatively | |
Secondary | Objective functional outcome in Knee Injury and Osteoarthritis Outcome Score (KOOS) | KOOS is a questionnaire designed to assess patient-relevant outcomes following knee injury. The KOOS assesses outcomes: pain, symptoms, activities of daily living, sport and recreation function, and knee-related quality of life. All items have five possible answer options scored from 0 (No problems) to 4 (Extreme problems). Scores between 0 and 100 represent the percentage of total possible score achieved. | 14-days, 3-, 6-, and 12- months postoperatively | |
Secondary | Cardiovascular events and/or surgical site or implants complications | Correlation of FINDRISC scale results with cardiovascular events and/or surgical site or implants complications | 12 months postoperatively |
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