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Determining the Suitability of Registries for Embedding Clinical Trials in the United States: A Project of the Clinical Trials Transformation Initiative.

Publication ,  Journal Article
Mikita, JS; Mitchel, J; Gatto, NM; Laschinger, J; Tcheng, JE; Zeitler, EP; Swern, AS; Flick, ED; Dowd, C; Lystig, T; Calvert, SB
Published in: Ther Innov Regul Sci
January 2021

BACKGROUND: Patient registries are organized systems that use observational methods to collect uniform data on specified outcomes in a population defined by a particular disease, condition, or exposure. Data collected in registries often coincide with data that could support clinical trials. Integrating clinical trials within registries to create registry-embedded clinical trials offers opportunities to reduce duplicative data collection, identify and recruit patients more efficiently, decrease time to database lock, accelerate time to regulatory decision-making, and reduce clinical trial costs. This article describes a project of the Clinical Trials Transformation Initiative (CTTI) intended to help clinical trials researchers determine when a registry could potentially serve as the platform for the conduct of a clinical trial. METHODS: Through a review of registry-embedded clinical trials and commentaries, semi-structured interviews with experts, and a multi-stakeholder expert meeting, the project team addressed how to identify and describe essential registry characteristics, practices, and processes required to for conducting embedded clinical trials intended for regulatory submissions in the United States. RESULTS: Recommendations, suggested practices, and decision trees that facilitate the assessment of whether a registry is suitable for embedding clinical trials were developed, as well as considerations for the design of new registries. Essential registry characteristics include relevancy, robustness, reliability, and assurance of patient protections. CONCLUSIONS: The project identifies a clear role for registries in creating a sustainable and reusable infrastructure to conduct clinical trials. Adoption of these recommendations will facilitate the ability to perform high-quality and efficient prospective registry-based clinical trials.

Duke Scholars

Published In

Ther Innov Regul Sci

DOI

EISSN

2168-4804

Publication Date

January 2021

Volume

55

Issue

1

Start / End Page

6 / 18

Location

Switzerland

Related Subject Headings

  • United States
  • Statistics & Probability
  • Reproducibility of Results
  • Registries
  • Humans
  • Data Collection
  • 4905 Statistics
  • 3214 Pharmacology and pharmaceutical sciences
  • 1117 Public Health and Health Services
  • 0104 Statistics
 

Citation

APA
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Mikita, J. S., Mitchel, J., Gatto, N. M., Laschinger, J., Tcheng, J. E., Zeitler, E. P., … Calvert, S. B. (2021). Determining the Suitability of Registries for Embedding Clinical Trials in the United States: A Project of the Clinical Trials Transformation Initiative. Ther Innov Regul Sci, 55(1), 6–18. https://doi.org/10.1007/s43441-020-00185-5
Mikita, J Stephen, Jules Mitchel, Nicolle M. Gatto, John Laschinger, James E. Tcheng, Emily P. Zeitler, Arlene S. Swern, et al. “Determining the Suitability of Registries for Embedding Clinical Trials in the United States: A Project of the Clinical Trials Transformation Initiative.Ther Innov Regul Sci 55, no. 1 (January 2021): 6–18. https://doi.org/10.1007/s43441-020-00185-5.
Mikita JS, Mitchel J, Gatto NM, Laschinger J, Tcheng JE, Zeitler EP, et al. Determining the Suitability of Registries for Embedding Clinical Trials in the United States: A Project of the Clinical Trials Transformation Initiative. Ther Innov Regul Sci. 2021 Jan;55(1):6–18.
Mikita, J. Stephen, et al. “Determining the Suitability of Registries for Embedding Clinical Trials in the United States: A Project of the Clinical Trials Transformation Initiative.Ther Innov Regul Sci, vol. 55, no. 1, Jan. 2021, pp. 6–18. Pubmed, doi:10.1007/s43441-020-00185-5.
Mikita JS, Mitchel J, Gatto NM, Laschinger J, Tcheng JE, Zeitler EP, Swern AS, Flick ED, Dowd C, Lystig T, Calvert SB. Determining the Suitability of Registries for Embedding Clinical Trials in the United States: A Project of the Clinical Trials Transformation Initiative. Ther Innov Regul Sci. 2021 Jan;55(1):6–18.
Journal cover image

Published In

Ther Innov Regul Sci

DOI

EISSN

2168-4804

Publication Date

January 2021

Volume

55

Issue

1

Start / End Page

6 / 18

Location

Switzerland

Related Subject Headings

  • United States
  • Statistics & Probability
  • Reproducibility of Results
  • Registries
  • Humans
  • Data Collection
  • 4905 Statistics
  • 3214 Pharmacology and pharmaceutical sciences
  • 1117 Public Health and Health Services
  • 0104 Statistics