Diabetes Mellitus Clinical Trial
Official title:
Incidence of Lactic Acidosis After Coronary Angiography and Angioplasty in Diabetic Patients on Continued Metformin Therapy With Normal Renal Function.
The purpose of this study is to determine whether metformin causes lactic acidosis in
diabetic patients with preserved kidney function, undergoing coronary angiography or
angioplasty with new contrast media.
In other words is it necessary to discontinue metformin before these procedures, even when
Iodixanol is used as contrast media, which is isosmolar agent and much more safer than
urografin which was the main agent in the previous studies that were the base of present
guidelines?
Although metformin is not directly nephrotoxic, it has been postulated that can impair
gluconeogenesis from lactate, which may lead to lactate accumulation under circumstances
such as acute renal failure. In diabetic patients receiving metformin, this condition can be
encountered in the setting of acute renal failure following contrast media administration,
during coronary angiography i.e. contrast-induced nephropathy. As a result, it has been a
part of routine clinical practice to discontinue metformin before angiography to prevent
metformin-associated lactic acidosis (MALA). However, there is no general consensus
regarding the incidence of MALA and evidence for such intervention is poor. On the other
hand, discontinuation of metformin can be associated with detrimental effects on glycemic
control and thereby may increase cardiovascular risk in diabetic patients undergoing
percutaneous coronary interventions. Consequently, questions have been raised recently
regarding the routine discontinuation of metformin, in low-risk patients undergoing coronary
angiography.
The present study was designed to assess the role of metformin in lactate production in a
group of diabetic patients with normal renal function; and to address the questions about
significance of routine discontinuation of metformin in low risk patients undergoing
coronary angiography.
Iodixanol will be the only contrast media in all patients, because of its low
nephrotoxicity. Serum blood urea nitrogen and creatinin; as well as arterial blood gases
will be evaluated prior to angiography, and repeated 24 and 48 hours after the procedure.
Glomerular filtration rate (GFR) is calculated using Cockcroft-Gault formula {GFR= 0.85 (for
women)}.
Contrast-induced acute kidney injury is defined as a 25-50% or 0.3-0.5 mg/dl net increase in
creatinine concentration compared to the baseline values. Metformin-associated lactic
acidosis (MALA) is defined as an arterial pH (potential of hydrogen)<7.35 and plasma lactate
concentration >5 mmol⁄L. In the M (-) group metformin will re-started 48 hours after
angiography, albeit in the absence of evidence of lactic acidosis and GFR of >60 mL/min per
1.73 m2.
A written informed consent is taken from all participants and institutional review board has
already approved the trial.
;
Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03743779 -
Mastering Diabetes Pilot Study
|
||
Completed |
NCT03786978 -
Pharmaceutical Care in the Reduction of Readmission Rates in Diabetes Melitus
|
N/A | |
Completed |
NCT01804803 -
DIgital Assisted MONitoring for DiabeteS - I
|
N/A | |
Completed |
NCT05039970 -
A Real-World Study of a Mobile Device-based Serious Health Game on Session Attendance in the National Diabetes Prevention Program
|
N/A | |
Completed |
NCT04507867 -
Effect of a NSS to Reduce Complications in Patients With Covid-19 and Comorbidities in Stage III
|
N/A | |
Completed |
NCT04068272 -
Safety of Bosentan in Type II Diabetic Patients
|
Phase 1 | |
Completed |
NCT03243383 -
Readmission Prevention Pilot Trial in Diabetes Patients
|
N/A | |
Completed |
NCT03730480 -
User Performance of the CONTOUR NEXT and CONTOUR TV3 Blood Glucose Monitoring System (BGMS)
|
N/A | |
Recruiting |
NCT02690467 -
Efficacy, Safety and Acceptability of the New Pen Needle 34gx3,5mm.
|
N/A | |
Completed |
NCT02229383 -
Phase III Study to Evaluate Safety and Efficacy of Added Exenatide Versus Placebo to Titrated Basal Insulin Glargine in Inadequately Controlled Patients With Type II Diabetes Mellitus
|
Phase 3 | |
Completed |
NCT05799976 -
Text Message-Based Nudges Prior to Primary Care Visits to Increase Care Gap Closure
|
N/A | |
Completed |
NCT06181721 -
Evaluating Glucose Control Using a Next Generation Automated Insulin Delivery Algorithm in Patients With Type 1 and Type 2 Diabetes
|
N/A | |
Recruiting |
NCT04489043 -
Exercise, Prediabetes and Diabetes After Renal Transplantation.
|
N/A | |
Withdrawn |
NCT03319784 -
Analysis for NSAID VS Corticosteroid Shoulder Injection in Diabetic Patients
|
Phase 4 | |
Completed |
NCT03542084 -
Endocrinology Auto-Triggered e-Consults
|
N/A | |
Completed |
NCT02229396 -
Phase 3 28-Week Study With 24-Week and 52-week Extension Phases to Evaluate Efficacy and Safety of Exenatide Once Weekly and Dapagliflozin Versus Exenatide and Dapagliflozin Matching Placebo
|
Phase 3 | |
Recruiting |
NCT05544266 -
Rare and Atypical Diabetes Network
|
||
Completed |
NCT01892319 -
An International Non-interventional Cohort Study to Evaluate the Safety of Treatment With Insulin Detemir in Pregnant Women With Diabetes Mellitus. Diabetes Pregnancy Registry
|
||
Completed |
NCT05031000 -
Blood Glucose Monitoring Systems: Discounter Versus Brand
|
N/A | |
Recruiting |
NCT04039763 -
RT-CGM in Young Adults at Risk of DKA
|
N/A |