Initial Results Submission

Information Program on Clinical Trials: Maintaining a Registry and Results Databank (NLM)

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0925-0586 can be found here:

Documents and Forms

Document Name Document Type
Form 2 Initial Results Submission Form and Instruction
2 ClinicalTrials.gov Results Reporting Data Entry Screen S Attachment 4 - ClinicalTrials.gov Results Reporting Data Entry Screen Shots.pdf Form and Instruction

Information Collection (IC) Details

IC Title:	Initial Results Submission	Agency IC Tracking Number:

Is this a Common Form? No		IC Status: Removed

Obligation to Respond: Voluntary

CFR Citation:

Information Collection Instruments:

Document Type	Form No.	Form Name	Instrument File	URL	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability
Form and Instruction	2	ClinicalTrials.gov Results Reporting Data Entry Screen Shots	Attachment 4 - ClinicalTrials.gov Results Reporting Data Entry Screen Shots.pdf		Yes	Yes	Fillable Fileable

Line of Business: Health

Subfunction: Consumer Health and Safety

Privacy Act System of Records
Title:	FR Citation:

Number of Respondents: 3,700	Number of Respondents for Small Entity: 0

Affected Public: Private Sector	Private Sector: Businesses or other for-profits

Percentage of Respondents Reporting Electronically: 100 %

	Program Change Due to Agency Discretion	Previously Approved
Annual Number of Responses for this IC	-3,700	3,700
Annual IC Time Burden (Hours)	-92,500	92,500
Annual IC Cost Burden (Dollars)	0	0

Documents for IC

Title	Document	Date Uploaded
No associated records found

Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.