# Proposed Collection: 30-Day Comment Request; The Clinical Trials Reporting Program (CTRP) Database (NCI)
**AGENCY:**
National Institutes of Health, HHS.
**ACTION:**
Notice.
**SUMMARY:**
In compliance with the requirement of the Paperwork Reduction Act of 1995 to provide an opportunity for public comment on proposed data collection projects, the National Institutes of Health, National Cancer Institute (NCI) will publish periodic summaries of proposed projects to be submitted to the Office of Management and Budget (OMB) for review and approval.
**DATES:**
Comments regarding this information collection are best assured of having their full effect if received by April 27, 2026.
**ADDRESSES:**
Written comments and recommendations for the proposed information collection should be sent within 30 days of publication of this notice to *www.reginfo.gov/public/do/PRAMain.* Find this particular information collection by selecting “Currently under 30-day Review—Open for Public Comments” or by using the search function.
**FOR FURTHER INFORMATION CONTACT:**
To request more information on the proposed project or to obtain a copy of the data collection plans and instruments, contact Melissa Park, PRA Liaison, Office of Management Policy and Compliance, National Cancer Institute, 9609 Medical Center Drive, Room 2E196, Bethesda, MD 20892 or call non-toll-free number (240) 276-5717 or email your request, including your address to: *[email protected].* Formal requests for additional plans and instruments must be requested in writing.
**SUPPLEMENTARY INFORMATION:**
This proposed information collection was previously published in the *Federal Register* on December 23, 2025 (Vol. 90, No. 244, FR 60112) and allowed 60 days for public comment. No public comments were received. The purpose of this notice is to allow an additional 30 days for public comment. The National Cancer Institute (NCI), National Institutes of Health, may not conduct or sponsor, and the respondent is not required to respond to, an information collection that has been extended, revised, or implemented on or after October 1, 1995, unless it displays a currently valid OMB control number.
In compliance with Section 3507(a)(1)(D) of the Paperwork Reduction Act of 1995, the National Institutes of Health (NIH) has submitted to the Office of Management and Budget (OMB) a request for review and approval of the information collection listed below.
*Proposed Collection Title:* The Clinical Trials Reporting Program (CTRP) Database, 0925-0600, Expiration Date 02/28/2026-REINSTATEMENT WITH CHANGE, National Cancer Institute (NCI), National Institutes of Health (NIH).
*Need and Use of Information Collection:* The Clinical Trials Reporting Program (CTRP) is an electronic resource that serves as a single, definitive source of information about all NCI-supported clinical research. This resource allows the NCI to consolidate reporting, aggregate data, and reduce redundant submissions. Clinical research administrators submit information as designees of clinical investigators who conduct NCI-supported clinical research. The designees can electronically access the CTRP website to complete the initial trial registration. After registration, three amendments and four study subject accrual updates occur per trial annually.
OMB approval is requested for three years. There are no costs to respondents other than their time. The estimated annualized burden hours are 18,000.
| Form name | Type of respondents | Number of | Number of | Average | Total annual burden hours |
| --- | --- | --- | --- | --- | --- |
| Initial Trial Registration | Individuals | 3,000 | 1 | 1 | 3,000 |
| Trial Registration Update | | 1,500 | 3 | 1 | 4,500 |
| Trial Registration Amendment | | 1,500 | 3 | 1 | 4,500 |
| Accrual Updates | | 3,000 | 4 | 30/60 | 6,000 |
| Totals | | 9,000 | 24,000 | | 18,000 |
Dated: March 24, 2026.
Melissa M. Park,
Project Clearance Liaison, National Cancer Institute, National Institutes of Health.