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  1. Home | ClinicalTrials.gov

    ClinicalTrials.gov is a website and online database of clinical research studies and information about their results. The National Library of Medicine (NLM) maintains the website.

  2. ClinicalTrials.gov PRS: Login

    See How to Apply on ClinicalTrials.gov for information on how to apply for a PRS account. See PRS Guided Tutorials for assistance with entering registration and results information in the PRS.

  3. ClinicalTrials.gov PRS: Home page (Beta)

    The National Library of Medicine (NLM) has launched an effort to modernize ClinicalTrials.gov. We will be continually delivering improvements throughout the modernization effort.

  4. ClinicalTrials.gov: Requirements and Implementation Strategies

    ClinicalTrials.gov was launched in February 2000 by the National Library of Medicine (NLM), a component of the National Institutes of Health (NIH). Since its launch, the policies and laws related to …

  5. - Overview - ClinicalTrials.gov

    Entering More Information: Certain Agreements and Results Point of Contact

  6. Jun 27, 2018 · The final rule for Clinical Trials Registration and Results Information Submission (42 CFR Part 11) specifies requirements for submitting clinical trial information to ClinicalTrials.gov.

  7. A randomized, double-blind, placebo-controlled, parallel-group, multicenter study to evaluate the safety and efficacy of secukinumab 300 mg and 150 mg in adult patients with active psoriatic arthritis after …

  8. Results information is submitted to ClinicalTrials.gov by the sponsor or investigator, and NLM staff assess for apparent errors, deficiencies, or inconsistencies.

  9. Jan 18, 2017 · Observational Study Protocol Registration Template ClinicalTrials.gov is a service of the National Institutes of Health For more information, see How to Register Your Study at …

  10. Jan 18, 2017 · ClinicalTrials.gov A service of the National Institutes of Health ... *Required *§ Required if Primary Completion Date is on or after January 18, 2017 [*] Conditionally required Adverse Event …