Studies With Patients
Date Revised: 07/15/02
National Institutes of Health
Access to the Protocol Registration System (PRS)
The National Institutes of Health (NIH)
through its National Library of Medicine (NLM) developed the Protocol
Registration System (PRS) to allow researchers and sponsors to list
current information about clinical trials. This data entry system is
restricted to authorized users, but operates to make information available
to the public as required by the 1997 FDA Revitalization Act. Please
visit http://clinicaltrials.gov
to view the information compiled by this system concerning the clinical
research being conducted or funded by NIH institutes.
"WARNING"
This page is for authorized users only.
If you are not authorized by NIAMS, please exit this page.
Welcome to the NIAMS Protocol Registration System(Formerly
called CTDB). Please review the data entry instructions below before
entering into the system.
- Questions and comments should be sent to me, NIAMS Administrator
at niamsctdb@mail.nih.gov.
-
Do not change the primary and secondary IDs. These have been entered
by NIAMS.
- Do not include any URLs. Only Institute approved URLs will be included.
- There are certain fields that are required by the FDA Revitalization Act
of 1997 and the NIH. These fields must be completed and are often
flagged as Error and Note messages. Please refer to the list
of NIAMS required fields, which are listed in the initial email.
- Please view your record and correct errors and notes before sending the data
back to me. Be sure that you have completed all of the fields
which NIAMS has required.
- When you are finished reviewing your data, change the status of the record
to complete. I will review your data for release to the general
public.
Please Enter the Protocol Registration System