{"id":9206,"date":"2017-02-21T14:43:00","date_gmt":"2017-02-21T22:43:00","guid":{"rendered":"https:\/\/www.washington.edu\/research\/?page_id=9206"},"modified":"2026-03-24T11:51:37","modified_gmt":"2026-03-24T18:51:37","slug":"how-to-register-a-clinical-trial","status":"publish","type":"page","link":"https:\/\/www.washington.edu\/research\/hsd\/clinical-trials\/how-to-register-a-clinical-trial\/","title":{"rendered":"How to Register a Clinical Trial on ClinicalTrials.gov"},"content":{"rendered":"<div class=\"table-of-contents\">\n<h3>Contents<\/h3>\n<ul class=\"list-unstyled\">\n<li style=\"list-style-type: none;\">\n<ul class=\"list-unstyled\">\n<li><a href=\"#PRS\">The Protocol Registration and Results System (PRS)<\/a><\/li>\n<li><a href=\"#who\">Who Can Use the 91爆料 PRS Organizational Account<\/a><\/li>\n<li><a href=\"#create\">Creating a User Account<\/a><\/li>\n<li><a href=\"#help\">General Help Documents to Get Started in the PRS<\/a><\/li>\n<li><a href=\"#roles\">PRS Roles and Responsibilities<\/a><\/li>\n<li><a href=\"#reg\">Registering a Trial<\/a><\/li>\n<li><a href=\"#tips\">Helpful Tips<\/a><\/li>\n<li><a href=\"#probs\">Resolving Problems<\/a><\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<\/div>\n<h2><a name=\"PRS\"><\/a>The Protocol Registration and Results System (PRS)<\/h2>\n<p>Clinical trials are registered on the\u202f<a href=\"https:\/\/clinicaltrials.gov\/\">ClinicalTrials.gov<\/a>\u202fsite through a web-based data entry system called the\u202f<a href=\"https:\/\/register.clinicaltrials.gov\/\">Protocol Registration and Results System (PRS)<\/a>. Some terms used in relation to accounts in the PRS include:<\/p>\n<ul>\n<li><strong>Organizational account.<\/strong> An organization (e.g., the 91爆料) has a single PRS organizational account. The 91爆料 account is called\u202f<strong>91爆料ashington<\/strong>.<\/li>\n<li><strong>Organization account manager.<\/strong> The\u202f<strong>91爆料ashington<\/strong>\u202faccount is managed by HSD\u2019s Regulatory Affairs team.<\/li>\n<li><strong>Individual user accounts.<\/strong> Researchers or their staff must set up\u202f<a href=\"https:\/\/www.washington.edu\/research\/policies\/sop-creating-a-ct-gov-user-account-2\/\">user accounts<\/a>\u202fthrough the organization account. An individual\u2019s user account may be used for more than one clinical trial.<\/li>\n<\/ul>\n<h2><a name=\"who\"><\/a>Who Can Use The 91爆料 PRS Organizational account<\/h2>\n<p aria-level=\"2\">Any 91爆料 faculty, staff or student who is <a href=\"https:\/\/www.washington.edu\/research\/policies\/sop-use-of-the-uw-irb-2\/\">eligible to use the 91爆料 IRB\u202f<\/a> for review of their studies may use the 91爆料 account to register clinical trials in which the 91爆料 is engaged in the research, even for trials that were reviewed by a non-91爆料 IRB instead of the 91爆料 IRB.<\/p>\n<h2><a name=\"create\"><\/a>Creating a User Account<\/h2>\n<p>To create your user account, following the instructions outlined in the <a href=\"https:\/\/www.washington.edu\/research\/policies\/sop-creating-a-ct-gov-user-account-2\/\">SOP Creating a CT.gov User Account<\/a>. Requests for a new user account are usually completed within 2 business days once the Regulatory Affairs team receives the request.<\/p>\n<h2><a name=\"help\"><\/a>General Help Documents to Get Started in the PRS<\/h2>\n<p>To assist researchers, HSD has linked to CT.gov Quick Overview Guides from the PRS site.<\/p>\n<ul>\n<li><strong>PRS Quick Overview Guides<\/strong>\n<ul class=\"revert-list-style\">\n<li><a href=\"https:\/\/cdn.clinicaltrials.gov\/documents\/tutorial\/content\/index.html#\/lessons\/sBqGs03CeGjGvrLw0ah5RlY1Yr5Ostgv\">Entering Initial Results and Uploading Study Documents<\/a><\/li>\n<li><a href=\"https:\/\/cdn.clinicaltrials.gov\/documents\/tutorial\/content\/index.html#\/lessons\/Cch5ChqjdCKS7MK2ga-vB2E54oj8kjvO\">Entering a New Registration<\/a><\/li>\n<li><a href=\"https:\/\/cdn.clinicaltrials.gov\/documents\/tutorial\/content\/index.html#\/lessons\/CBeLCSrW2M5pXLjeHsKuRPoO0_zhWML1\">Updating a Study Record<\/a><\/li>\n<\/ul>\n<\/li>\n<li><a href=\"https:\/\/register.clinicaltrials.gov\/prs\/html\/prs-users-guide.html\" target=\"_blank\" rel=\"noopener noreferrer\">PRS User&#8217;s Guide<\/a>: 28-pages of step-by-step instructions for how to use PRS<\/li>\n<\/ul>\n<h2><a name=\"roles\"><\/a>PRS Roles and Responsibilities<\/h2>\n<p>General information on different PRS roles and responsibilities can be found in section 3.1 of the <a href=\"https:\/\/register.clinicaltrials.gov\/prs\/html\/prs-users-guide.html\">PRS User\u2019s Guide<\/a>. The following provides 91爆料-specific information:<\/p>\n<p><strong>Sponsor (or Sponsor Organization) <\/strong>&#8211; The 91爆料 is a Sponsor Organization; it is listed in the PRS system as\u202f<strong>91爆料ashington<\/strong>.<\/p>\n<p><strong>Administrator <\/strong>&#8211; HSD\u2019s Regulatory Affairs team serves as the Administrator for the 91爆料ashington account.\u202fContact them through\u202f<a href=\"mailto:hsdreprt@uw.edu\">hsdreprt@uw.edu<\/a>.<\/p>\n<p><strong>Responsible Party <\/strong>&#8211; The <strong>91爆料 PI<\/strong> should be identified as the Responsible Party for studies reviewed by HSD. For studies managed under the Fred Hutch\/91爆料 Cancer Consortium, a PI who initiates or conducts an investigator-initiated clinical trial is designated as the Responsible Party, but the Responsible Party for other types of interventional trials is usually the Sponsor.<\/p>\n<h2><a name=\"reg\"><\/a>Registering a Trial<\/h2>\n<p>HSD reviews all incoming IRB applications and certain study modifications to determine whether the study is required to register and report results on CT.gov. The Regulatory Affairs staff at HSD will send an email to the study team if the trial meets these requirements and outline the steps for completing registration.<\/p>\n<p>If the study is required to register in PRS, Regulatory Affairs staff will initiate the trial registration for the PI in PRS. The PI will need to complete the registration in PRS no later than 21 days after enrollment of the first study participant or within 1 year of IRB approval (HSD Policy), whichever occurs first. <em><strong>Registration is completed when a National Clinical Trial (NCT) number has been assigned to the study record.<\/strong><\/em><\/p>\n<p>Generally, each IRB application will have its own PRS study registration. However, contact HSD at\u202f<a href=\"mailto:hsdreprt@uw.edu\">hsdreprt@uw.edu<\/a>\u202fregarding unique situations that may require more than one study registration for a study (e.g., NIH requests two separate registrations). Include \u2018<strong>CT.gov<\/strong>\u2019\u202fin the subject line of your email to help triage your message efficiently.<\/p>\n<h3>Registration Data Entry<\/h3>\n<p>After receiving the email from the Regulatory Affairs staff regarding initiation of trial registration, log into the <a href=\"https:\/\/register.clinicaltrials.gov\/\">PRS system<\/a> to enter data and complete registration. Information is entered by the study team in the trial record by completing a series of topic-specific sections (called modules) in the \u2018Protocol Section\u2019 located on the \u2018Record Summary\u2019 page.<\/p>\n<p>The following documents and links provide guidance and instructions on how to enter data into the modules:<\/p>\n<ul>\n<li><a href=\"https:\/\/www.washington.edu\/research\/forms-and-templates\/worksheet-clinical-trial-registration\/\">WORKSHEET Clinical Trial Registration<\/a>\u202fwas prepared by HSD for researchers. It lists the protocol modules and the specific data elements in each module. This allows the record creator to see in advance what specific information will be required, before going into the PRS system.<\/li>\n<\/ul>\n<p>Additional resources from CT.gov:<\/p>\n<ul>\n<li><strong>CT.gov PRS <a href=\"https:\/\/cdn.clinicaltrials.gov\/documents\/tutorial\/content\/index.html#\/\">Guided Tutorials<\/a><\/strong>\n<ul class=\"revert-list-style\">\n<li>Review section \u201cRegistration Tutorials\u201d which describes how to enter data in each individual module.<\/li>\n<\/ul>\n<\/li>\n<li><strong>CT.gov <a href=\"https:\/\/register.clinicaltrials.gov\/prs\/html\/prs-users-guide.html\">PRS User Guide<\/a><\/strong>\n<ul class=\"revert-list-style\">\n<li><a href=\"https:\/\/register.clinicaltrials.gov\/prs\/html\/prs-users-guide.html#Descriptionofprotocol\">2.1 &#8211; Description of Protocol Registration and Results System Workflow<\/a><\/li>\n<li><a href=\"https:\/\/register.clinicaltrials.gov\/prs\/html\/prs-users-guide.html#creatingnewrecordsec4\">4 &#8211; Creating a New Record and Entering Data<\/a><\/li>\n<li><a href=\"https:\/\/register.clinicaltrials.gov\/prs\/html\/prs-users-guide.html#section5\">5 &#8211; Preparing, Approving, and Releasing a Study Record to PRS<\/a><\/li>\n<li><a href=\"https:\/\/register.clinicaltrials.gov\/prs\/html\/prs-users-guide.html#section6\">6 &#8211; PRS Review Process<\/a><\/li>\n<\/ul>\n<\/li>\n<li><strong><a href=\"https:\/\/clinicaltrials.gov\/policy\/protocol-definitions\">PRS Protocol Registration Data Element Definitions<\/a><\/strong>. This PRS webpage provides definitions for each of the protocol registration data elements and indicates whether each element is required.<\/li>\n<li><a href=\"https:\/\/clinicaltrials.gov\/submit-studies\/prs-help\/protocol-registration-quality-control-review-criteria\"><strong>PRS Review Criteria for Registration<\/strong><\/a>\u202fdescribes the criteria used by the PRS system to assess completeness and consistency of results reporting.<\/li>\n<\/ul>\n<h2><a name=\"tips\"><\/a>Helpful Tips<\/h2>\n<ul>\n<li><strong>Smart forms.<\/strong> The PRS data entry forms are \u201csmart\u201d. This means that some fields will appear (or not) depending upon your answers to other questions.<\/li>\n<li><strong>Optional elements.<\/strong> A symbol, as described in the <a href=\"https:\/\/register.clinicaltrials.gov\/prs\/html\/definitions.html\">PRS Protocol Registration Data Element Definitions<\/a>, and shown below, indicates whether each data element is optional or required.<\/li>\n<\/ul>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"size-full wp-image-60624 aligncenter\" src=\"https:\/\/www.washington.edu\/research\/wp-content\/uploads\/PRS-optional-element.png\" alt=\"PRS optional elements diagram showing symbols that indicate whether a question is required\" width=\"412\" height=\"130\" srcset=\"https:\/\/www.washington.edu\/research\/wp-content\/uploads\/PRS-optional-element.png 412w, https:\/\/www.washington.edu\/research\/wp-content\/uploads\/PRS-optional-element-300x95.png 300w, https:\/\/www.washington.edu\/research\/wp-content\/uploads\/PRS-optional-element-375x118.png 375w\" sizes=\"auto, (max-width: 412px) 100vw, 412px\" \/><\/p>\n<ul>\n<li><strong>Special characters, formatting tips.<\/strong> See 4.2 Data Entry Tips in the <a href=\"https:\/\/register.clinicaltrials.gov\/prs\/html\/prs-users-guide.html\">PRS User\u2019s Guide<\/a> for help on formatting and using special character information (e.g., example: \u2264 or \u00b1).<\/li>\n<li><strong>One or multiple sessions.<\/strong> You do not need to complete the registration in one sitting. Use the save option at the bottom of the section where you are entering information before navigating away. When ready, log back in and return to any remaining sections to complete the registration.<\/li>\n<li><strong>Downloading a copy of the record.<\/strong> Section 5.1 of the <a href=\"https:\/\/register.clinicaltrials.gov\/prs\/html\/prs-users-guide.html\">PRS User\u2019s Guide<\/a> describes how to download an RTF file of your record. This can then be imported into Microsoft Word (or another word processing program) \u2013 which is very useful for editing and sharing a record with co-workers.<\/li>\n<li><strong>HIGHLY RECOMMENDED: Review what you have entered before you submit the record.<\/strong> Section 5.1 of the <a href=\"https:\/\/register.clinicaltrials.gov\/prs\/html\/prs-users-guide.html\">PRS User\u2019s Guide<\/a> describes several different ways to check your record. The <a href=\"https:\/\/prsinfo.clinicaltrials.gov\/ProtocolDetailedReviewItems.pdf\">PRS Protocol Review Criteria<\/a> document is also useful.<\/li>\n<\/ul>\n<h2><a name=\"probs\"><\/a>Resolving Problems<\/h2>\n<p>Section 8 of the <a href=\"https:\/\/register.clinicaltrials.gov\/prs\/html\/prs-users-guide.html\">PRS User\u2019s Guide<\/a> describes how to identify and resolve records with problems.<\/p>\n<p>For specific questions related to data entry or registration issues for your specific trial, we recommend contacting <a href=\"mailto:register@clinicaltrials.gov\">register@clinicaltrials.gov<\/a> for assistance.<\/p>\n<p>For general questions, contact HSD at <a href=\"mailto:hsdreprt@uw.edu\">hsdreprt@uw.edu<\/a> for assistance. Include \u2018<strong>CT.gov\u2019<\/strong> in the subject line of your email to help triage your message efficiently.<\/p>\n<p>For assistance with studies managed by the Cancer Consortium\u2019s Clinical Research Support (CRS) Office, contact CRS at <a href=\"mailto:CTgov@fredhutch.org\">CTgov@fredhutch.org<\/a>. More information can also be found on the <a href=\"https:\/\/www.cancerconsortium.org\/research-support\/clinical-research-support\/resources\/clinical-trial-registries.html\">CRS webpage<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Contents The Protocol Registration and Results System (PRS) Who Can Use the 91爆料 PRS Organizational Account Creating a User Account General Help Documents to Get Started&#8230;<\/p>\n","protected":false},"author":117,"featured_media":0,"parent":9197,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"templates\/page-builder-units-small-hero.php","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-9206","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.1.1 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>How to Register a Clinical Trial on ClinicalTrials.gov - 91爆料 Research<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.washington.edu\/research\/hsd\/clinical-trials\/how-to-register-a-clinical-trial\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"How to Register a Clinical Trial on ClinicalTrials.gov - 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