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Replication of the GRADE Diabetes Trial in Healthcare Claims Data

Replication of the GRADE Diabetes Trial in Healthcare Claims Data

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05099198
Enrollment
6403
Registered
2021-10-29
Start date
2018-09-01
Completion date
2021-08-01
Last updated
2023-07-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes

Brief summary

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.

Detailed 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.

Interventions

DRUGSitagliptin

Sitagliptin dispensing claim is used as the reference

DRUGGlimepiride

Glimepiride dispensing claim is used as the reference

Sponsors

Brigham and Women's Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
30 Years to No maximum
Healthy volunteers
No

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 \[-30, 0\]

Design outcomes

Primary

MeasureTime frameDescription
Time until failure to maintain metabolic controlThrough censoring or study completion, up to 765 days after cohort entryLab based algorithm: time until failure to maintain metabolic control (HbA1c level \>= 7.0% or 53 mmol/mol)

Secondary

MeasureTime frameDescription
Time until a severe hypoglycemic episodeThrough censoring or study completion, up to 765 day after cohort entryClaims based algorithm: time until a severe hypoglycemic episode
HbA1C change from baselineThrough censoring or study completion, up to 765 days after cohort entryLab based algorithm: HbA1C change from baseline

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026