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Replication of the GRADE Diabetes Trial in Healthcare Claims Data

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Mass General Brigham

Status

Completed

Conditions

Diabetes

Treatments

Drug: Sitagliptin
Drug: Glimepiride

Study type

Observational

Funder types

Other

Identifiers

NCT05099198
2018P002966-DUP-GRADE

Details and patient eligibility

About

Investigators are building an empirical evidence base for real world data through large-scale replication of randomized controlled trials. The investigators' goal is to understand for what types of clinical questions real world data analyses can be conducted with confidence and how to implement such studies.

Full description

This is a non-randomized, non-interventional study that is part of the RCT DUPLICATE initiative (www.rctduplicate.org) of the Brigham and Women's Hospital, Harvard Medical School. It is intended to replicate, as closely as is possible in healthcare insurance claims data, the trial listed below/above. Although many features of the trial cannot be directly replicated in healthcare claims, key design features, including outcomes, exposures, and inclusion/exclusion criteria, were selected to proxy those features from the trial. Randomization is also not replicable in healthcare claims data but was proxied through a statistical balancing of measured covariates according to standard practice. Investigators assume that the RCT provides the reference standard treatment effect estimate and that failure to replicate RCT findings is indicative of the inadequacy of the healthcare claims data for replication for a range of possible reasons and does not provide information on the validity of the original RCT finding.

Enrollment

6,403 patients

Sex

All

Ages

30+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age greater or equal than 30: days [0,0]
  • Diagnosis of Type 2 Diabetes: days [- All Data, 0]
  • 2+ recorded HbA1c levels: days [-365,0]
  • Metformin use: days [-30, 0]

Exclusion criteria

  • Type 1 or Secondary DM: days [-All Data, 0]
  • Previous organ transplant: days [-All Data, 0]
  • HIV/AIDS: days [-All Data, 0]
  • History of bariatric surgery: days [-All Data, 0]
  • Congestive heart failure: days [-All Data, 0]
  • NYHA >=3: days [-All Data, 0]
  • Pancreatitis: days [-All Data, 0]
  • Medullary thyroid cancer/MEN-2: days [-All Data, 0]
  • History of MI: days [-365, 0]
  • Stroke: days [-365, 0]
  • Coronary Revascularization: days [-365, 0]
  • PTCA/Stenting/CABG: days [-365, 0]
  • Trans myocardial revascularization: days [-365, 0]
  • Carotid bypass: days [-365, 0]
  • Cerebrovascular revascularization: days [-365, 0]
  • PVD: days [-365, 0]
  • CCI >=10: days [-365, 0]
  • History of cancer, other than non-melanoma skin cancer: days [-1,825, 0]
  • Treatment of metformin more than 10 years: days [-3,650, 0]
  • Treatment with any diabetes drug other than metformin; PCOS; symptomatic hyperglycemia; pregnancy; gestational diabetes: days [-180, 0]
  • History of hemolytic anemia; history of severe liver disease; current alcoholism; chronic transfusion requirement; ESRD: days [-180, 0]
  • Oral, IV, or IM cortisone, hydrocortisone, prednisone, methylprednisone, or dexamethasone: days [-90, 0]
  • Treatment with atypical antipsychotics, language barriers, nursing home, or missing age or gender: days {-180, 0]
  • Hospitalization with length of stay >3 days: days [-30, 0]

Trial design

6,403 participants in 2 patient groups

Sitagliptin
Description:
Reference group
Treatment:
Drug: Sitagliptin
Glimepiride
Description:
Exposure group
Treatment:
Drug: Glimepiride

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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