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UCSF Research Participant Registry

NCT01717378 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 1541

Last updated 2015-03-11

No results posted yet for this study

Summary

The UCSF Clinical and Translational Science Institute (CTSI) Consultation Service provides recruitment services and facilitates the enrollment of research participants into UCSF clinical studies. The Recruitment Services will be accessible to all researchers at UCSF and affiliated institutions and will address the common problems that investigators encounter in the recruitment process.

Recruitment Services considered and integrated Committee on Human Research (CHR) and HIPAA regulations for ensuring human subject rights, participant privacy, and data security into the recruitment workflow and data collection/extraction methods. Recruitment Services, therefore, requests approval to implement these processes systematically for all studies that have already obtained CHR approval to begin recruitment activities.

Conditions

  • Any Disease or Condition
  • Healthy

Sponsors & Collaborators

Principal Investigators

  • Deborah G Grady, MD, MPH,FACP · Clinical & Translational Science Institute, University of California San Francisco

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-03-31
Primary Completion
2015-02-28
Completion
2015-02-28

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01717378 on ClinicalTrials.gov