Reporting Guidelines for Pathology in Randomised Controlled Trials (CONSORT-Path)

Clinical Trials

The CONSORT-Path Core Delivery and Advisory groups propose to create an extension to the CONSORT statement to define the minimum reporting of pathology items within a study.

The guideline development process follows the methodology recommended by the EQUATOR network and will consist of the following phases:

  1. A systematic review of existing guidance relating to the practice of pathology within clinical trials and the creation of a unified item list.
  2. Consensus modified Delphi process informed by the systematic review unified item list.
  3. Final consensus meeting. An international group of diverse stakeholders, including clinical trialists of all specialities, regulators, journal editors, industry and patient partners will produce the final elements defining the CONSORT-Path standards. Planned for Spring 2022.

Registered: 4 June 2020

Last updated:

Contact: Dr Tim Kendall; Dr Max Robinson Email: [email protected]; [email protected]