Margaret Izabella Chustecki, MD, MBA
About
Biography
Margaret I. Chustecki is an Associate Clinical Professor at Yale School of Medicine. Born in Warsaw, Poland, and educated at Warsaw Medical School, she completed her internship and residency at Newton Wellesley Hospital and New England Medical Center. Before joining the Department of Internal Medicine at YSM as a Clinical Instructor, Dr. Chustecki had experience working as an Attending in both inpatient and outpatient settings. Prior to starting her own internal medical practice in 2003, she worked as an Attending for the Hospitalist Service at Yale New Haven Hospital.
Dr. Chustecki completed her MBA program at the Yale School of Management in 2009. This contributed to her developing and leading a medical practice (Internal Medicine of Greater New Haven). Her medical team aims to improve efficiency, performance and communication with patients and the public. She has implemented a quality program that achieved NCQA accreditation in eligible markets, and supported a quality infrastructure for additional programs, such as Meaningful Use and PQRS. She maintains her own clinical practice within the group practice. She coordinates the team of medical providers to support medical education and collect data to improve patient outcomes, manage costs and improve the quality of healthcare.
As an attending Dr. Chustecki has taught interns and residents at YNHH for many years. She has also taught and supervised medical students, PA students, and ad hoc residents from YNHH in Internal Medicine of Greater New Haven offices.
Appointments
Internal Medicine
Assistant Clinical ProfessorPrimary
Other Departments & Organizations
Education & Training
- MBA
- Yale School of Management (2009)
- MD
- Medical School (1988)
Research
Overview
Dr. Chustecki was involved in the following clinical trials:
- A Randomized, Double-Blind Study to Compare the Efficacy and Safety of Fixed Low Doses of Coumadin plus Aspirin to Aspirin Alone in the Prevention of Reinfarction, Cardiovascular Death and Stroke in Post Myocardial Infarction Patient
- Evaluation of Autonomic Function by Heart Rate Variability in Patients with Mitral Valve Prolapse
- Correlation of Platelet Activation, Platelet PADGEM Expression during Percutaneous Transluminal Angioplasty with Rate of Early Restenosis
- Response to T-pa Therapy in Transgenic Mice with Human Apolipoprotein Measured by Nuclear Scan
- Establishing Value as a Lescol Usage and Treatment Efficacy
- Research on the Effects of Aceon Tablets in Hypertensive Subjects in a Community Trial
- Cardiazem LA P.L.A.C.E. Program
- A Long-Term Outcomes Study to Assess Statin Residual Risk Reduction with XXXXX in High Cardiovascular Risk Patients with Hypertriglyceridemia
- A Multi-Centre, Randomized, Double-Blind, Active-Controlled, Parallel Group, Phase III Trial to Evaluate the Safety and Efficacy of Add-On Therapy with XXXXX and XXXXX added to Metformin compared to Add-On Therapy with XXXXX in combination with Metformin or XXXXX in combination with Metformin in Patients with Type 2 Diabetes who have Inadequate Glycaemic Control on Metformin Alone
- A Randomized, 12-Week, Double-Blind, Placebo-Controlled Study of the Safety and Efficacy of XXXXX in Patients with Irritable Bowel Syndrome with Constipation (IBS-C)
- A Randomized, Double-Blind, Parallel Group, Multi-Center Study to Assess the Efficacy and Safety of XXXXX Compared to XXXXX, XXXXX, and XXXXX, as an Active Control, on Lung Function over a 24-Week Treatment Period in Subjects With Moderate to Very Severe COPD
- An Open-Label, Long-Term Safety and Tolerability Study of XXXXX in Patients with Irritable Bowel Syndrome with Constipation (IBS-C)
- A Parallel Group, Double-Blind, Randomized, Placebo Controlled, Trial to Evaluate the Efficacy and Safety of XXXXX Administered Intravenously in Patients with Migraines
- A Randomized Parallel-Group, Placebo-Controlled, Double-Blind, Event-Driven, Multi- Center Pivotal Phase III Clinical Outcome Trial of Efficacy and Safety of the XXXXX in Subjects With Heart Failure With Reduced Ejection Fraction (HFrEF) –XXXXX Global Study in Subjects With Heart Failure With Reduced Ejection Fraction (XXXXX)
- A Multicenter Study Conducted to Evaluate the Performance of the XXXXX Test in Laboratory and Point of Care Testing Sites
- A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO ASSESS THE EFFECTS OF XXXXX ON THE OCCURRENCE OF MAJOR CARDIOVASCULAR EVENTS IN PATIENTS WITH, OR AT HIGH RISK FOR, CARDIOVASCULAR DISEASE WHO ARE STATIN INTOLERANT
- A RANDOMIZED, DOUBLE-BLIND, PARALLEL GROUP, MULTICENTER STUDY TO EVALUATE THE EFFICACY AND SAFETY OF XXXXX COMPARED TO XXXXX ADDED TO BACKGROUND LIPID-MODIFYING THERAPY IN PATIENTS WITH ELEVATED LDL-C WHO ARE STATIN INTOLERANT
- AN OPEN-LABEL, RANDOMIZED, MULTICENTER, PHASE III STUDY TO COMPARE THE IMMUNOGENICITY, EFFICACY, AND SAFETY OF GAN & LEE PHARMACEUTICALS XXXXX INJECTION TO XXXXX (XXXXX INJECTION) IN ADULT SUBJECTS WITH TYPE 1 DIABETES MELLITUS
- AN OPEN-LABEL, RANDOMIZED, MULTICENTER, PHASE III STUDY TO COMPARE THE IMMUNOGENICITY, EFFICACY, AND SAFETY OF GAN & LEE PHARMACEUTICALS INSULIN XXXXX INJECTION TO XXXXX (XXXXX INJECTION) IN ADULT SUBJECTS WITH TYPE 2 DIABETES MELLITUS
- A Phase 2a Randomized, Double-blind, Placebo-controlled, Parallel-designed Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamic Effects of XXXXX in Subjects with Stable Coronary Heart Disease
- A Phase 2, Double-Blind, Placebo-Controlled, 3-Month Trial of XXXXX versus XXXXX in Patients with Type 2 Diabetes Mellitus
- A Phase 2 Study of Once-Weekly XXXXX Compared with XXXXX and XXXXX in Patients with Type 2 Diabetes Mellitus
- A Phase 2, 24-Week, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Safety and Efficacy of XXXXX for the Treatment of Moderately to Severely Symptomatic Knee Osteoarthritis
- A Phase 3, Multicenter, Observational Long-term Study Evaluating the Safety, Tolerability, and Efficacy of Treatment of XXXXX or XXXXX Previously Injected in the Target Knee Joint of Subjects with Moderately to Severely Symptomatic Osteoarthritis
- XXXXX TO REDUCE CARDIOVASCULAR OUTCOMES BY REDUCING TRIGLYCERIDES IN PATIENTS WITH DIABETES (XXXXX)
- Efficacy and Safety of Fast-acting Insulin XXXXX Compared to XXXXX both in Combination with Insulin XXXXX with or without XXXXX in Adults with Type 2 Diabetes
- A trial comparing the efficacy and safety of insulin XXXXX and insulin XXXXX in subjects with type 2 diabetes mellitus inadequately treated with basal insulin, with or without oral antidiabetic drugs
- Phase 4/post-marketing - A randomised, cross-over, open-label, multi-centre trial comparing the effect of XXXXX and XXXXX, with or without XXXXX in subjects with type 2 diabetes using flash glucose monitoring
- A 26-week randomized, open-label, active-controlled, 2-treatment arm, parallel group multi-center study, comparing the efficacy and safety of XXXXX versus XXXXX in ethnically/racially diverse patients with type 2 diabetes mellitus inadequately controlled on basal insulin and oral antidiabetic agents Phase 3b
- A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Effect of XXXXX on Cardiovascular Outcomes in Type 2 Diabetes Patients at High Cardiovascular Risk
- A Randomized, Double-Blind, Parallel Group, Multi-Center 24-Week Study Comparing the Efficacy and Safety of Three Doses of XXXXX to XXXXX and XXXXX in Subjects With Persistent Asthma
- A Phase 3 Randomized, Double-blind, Placebo-controlled, Multi-center Study to Evaluate the Efficacy and Safety of XXXXX in Combination With the Standard-of-care Treatment in Adolescent, Adult, and Elderly Non-hospitalized Subjects With Influenza A Infection who Are at Risk of Developing Complications
- A Randomized, Double-Blind, Parallel Group, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Tolerability of Single Doses of XXXXX in the Acute Treatment of Migraine
- A Phase 2 Multi-Center, Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Safety of XXXXX in Patients with New Onset or Established Type 1 Diabetes Mellitus (XXXXX)
- A Phase 3 Randomized, Double-blind, Multi-dose, Placebo and NSAID-controlled Study to Evaluate the Efficacy and Safety of XXXXX in Patients with Pain Due to Osteoarthritis of the Knee or Hip
- Efficacy and Safety of XXXXX Once Weekly versus XXXXX in Patients with Type 2 Diabetes and Increased Cardiovascular Risk (XXXXX)
- XXXXX TO REDUCE CARDIOVASCULAR OUTCOMES BY REDUCING TRIGLYCERIDES IN PATIENTS WITH DIABETES (XXXXX)
- A Phase 3, Randomized, Open-Label Trial Comparing Efficacy and Safety of XXXXX versus XXXXX Once Weekly as Add-on Therapy to XXXXX in Patients with Type 2 Diabetes (XXXXX)
- A Phase 2, Randomized, Double-blind, Placebo-controlled, Parallel-group, Dose-range-finding Study of XXXXX Administered Orally for 12 Weeks to Treat Abdominal Pain in Patients with Diarrhea-predominant Irritable Bowel Syndrome
- A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multicenter Study Evaluating the Efficacy and Safety of XXXXX in Subjects with Moderate to Advanced Diabetic Kidney Disease
- Evaluation of the XXXXX Test in an Average Patient Screening Episode (XXXXX)
- A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Parallel-Group Study to Evaluate the Efficacy and Safety of XXXXX in Subjects with Diabetic Peripheral Neuropathic Pain
- Reference Population Interval Evaluation with Access XXXXX Enrollment and Specimen Collection
- The Effect of XXXXX versus XXXXX plus standard of care on Major Cardiovascular Events in Patients with Type 2 Diabetes
- A Study to Support the Radiographic Eligibility Screening Process of XXXXX Studies in Symptomatic Knee Osteoarthritis Subjects
- A Phase 3, 28-Week, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of a Single Injection of XXXXX Injected in the Target Knee Joint of Moderately to Severely Symptomatic Osteoarthritis Subjects
- A Study of XXXXX in Participants with Type 2 Diabetes using Continuous Glucose Monitoring
- A Double-Blinded, Placebo-controlled, Double Dummy, Multi-center Randomized, Phase 3 Study to Evaluate the Efficacy and Safety of XXXXX in Subjects with Type 2 Diabetes Mellitus with Inadequate Glycemic Control on Two or Three Oral Glucose-lowering Agents
- A Phase 2/3 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Oral XXXXX in Migraine Prevention
- A Post Approval Study to Evaluate the Safety of the Eversense® Continuous Glucose Monitoring (CGM) System Used Non-adjunctively
- A Master Protocol for Randomized, Placebo-Controlled, Phase 2 Clinical Trials of Multiple Interventions for the Treatment of Chronic Pain
- Randomized, Placebo-Controlled, Phase 2 Clinical Trial to Evaluate XXXXX for the Treatment of Diabetic Peripheral Neuropathic Pain
- Randomized, Placebo-Controlled, Phase 2 Clinical Trial to Evaluate XXXXX for the Treatment of Osteoarthritis Pain
- A Phase 3, Parallel-Design, Open-Label, Randomized Controlled Study to Evaluate the Efficacy and Safety of XXXXX as a Weekly Basal Insulin Compared to XXXXX in Adults with Type 2 Diabetes on Multiple Daily Injections
- A Phase 4, Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Efficacy and Safety of XXXXX Versus XXXXX in Adult Participants with Episodic Migraine
- A Phase 3, Open-label, Multi-center, Single-arm Study to Assess Contraceptive Efficacy and Safety of the XXXXX + XXXXX Combined Oral Contraceptive (XXXXX) in Premenopausal Females Aged 14 to 35 Years (Inclusive)
- Evaluation of the XXXXX Test in an Average Patient Screening Episode (XXXXX)