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INFORMATION FOR

    Voluntary Faculty

    Voluntary faculty are typically clinicians or others who are employed outside of the School but make significant contributions to department programs at the medical center or at affiliate institutions.

    Voluntary rank details

    Margaret Izabella Chustecki, MD, MBA

    she/her/hers
    Associate Clinical Professor
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    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.

    Last Updated on October 09, 2024.

    Appointments

    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:

    1. 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
    2. Evaluation of Autonomic Function by Heart Rate Variability in Patients with Mitral Valve Prolapse
    3. Correlation of Platelet Activation, Platelet PADGEM Expression during Percutaneous Transluminal Angioplasty with Rate of Early Restenosis
    4. Response to T-pa Therapy in Transgenic Mice with Human Apolipoprotein Measured by Nuclear Scan
    5. Establishing Value as a Lescol Usage and Treatment Efficacy
    6. Research on the Effects of Aceon Tablets in Hypertensive Subjects in a Community Trial
    7. Cardiazem LA P.L.A.C.E. Program
    8. A Long-Term Outcomes Study to Assess Statin Residual Risk Reduction with XXXXX in High Cardiovascular Risk Patients with Hypertriglyceridemia
    9. 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
    10. 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)
    11. 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
    12. An Open-Label, Long-Term Safety and Tolerability Study of XXXXX in Patients with Irritable Bowel Syndrome with Constipation (IBS-C)
    13. A Parallel Group, Double-Blind, Randomized, Placebo Controlled, Trial to Evaluate the Efficacy and Safety of XXXXX Administered Intravenously in Patients with Migraines
    14. 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)
    15. A Multicenter Study Conducted to Evaluate the Performance of the XXXXX Test in Laboratory and Point of Care Testing Sites
    16. 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
    17. 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
    18. 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
    19. 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
    20. 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
    21. A Phase 2, Double-Blind, Placebo-Controlled, 3-Month Trial of XXXXX versus XXXXX in Patients with Type 2 Diabetes Mellitus
    22. A Phase 2 Study of Once-Weekly XXXXX Compared with XXXXX and XXXXX in Patients with Type 2 Diabetes Mellitus
    23. 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
    24. 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
    25. XXXXX TO REDUCE CARDIOVASCULAR OUTCOMES BY REDUCING TRIGLYCERIDES IN PATIENTS WITH DIABETES (XXXXX)
    26. 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
    27. 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
    28. 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
    29. 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
    30. 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
    31. 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
    32. 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
    33. 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
    34. 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)
    35. 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
    36. Efficacy and Safety of XXXXX Once Weekly versus XXXXX in Patients with Type 2 Diabetes and Increased Cardiovascular Risk (XXXXX)
    37. XXXXX TO REDUCE CARDIOVASCULAR OUTCOMES BY REDUCING TRIGLYCERIDES IN PATIENTS WITH DIABETES (XXXXX)
    38. 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)
    39. 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
    40. 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
    41. Evaluation of the XXXXX Test in an Average Patient Screening Episode (XXXXX)
    42. 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
    43. Reference Population Interval Evaluation with Access XXXXX Enrollment and Specimen Collection
    44. The Effect of XXXXX versus XXXXX plus standard of care on Major Cardiovascular Events in Patients with Type 2 Diabetes
    45. A Study to Support the Radiographic Eligibility Screening Process of XXXXX Studies in Symptomatic Knee Osteoarthritis Subjects
    46. 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
    47. A Study of XXXXX in Participants with Type 2 Diabetes using Continuous Glucose Monitoring
    48. 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
    49. A Phase 2/3 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Oral XXXXX in Migraine Prevention
    50. A Post Approval Study to Evaluate the Safety of the Eversense® Continuous Glucose Monitoring (CGM) System Used Non-adjunctively
    51. A Master Protocol for Randomized, Placebo-Controlled, Phase 2 Clinical Trials of Multiple Interventions for the Treatment of Chronic Pain
    52. Randomized, Placebo-Controlled, Phase 2 Clinical Trial to Evaluate XXXXX for the Treatment of Diabetic Peripheral Neuropathic Pain
    53. Randomized, Placebo-Controlled, Phase 2 Clinical Trial to Evaluate XXXXX for the Treatment of Osteoarthritis Pain
    54. 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
    55. A Phase 4, Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Efficacy and Safety of XXXXX Versus XXXXX in Adult Participants with Episodic Migraine
    56. 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)
    57. Evaluation of the XXXXX Test in an Average Patient Screening Episode (XXXXX)

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