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IRB NUMBER: 2108072FB IRB APPROVAL DATE: 07/26/2022 IRB EXPIRATION DATE: 05/19/2023Main Consent Form Quantifying the impact of the peanut ball on the duration of the active stage of labor. PRINCIPAL

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How to fill out classic clinicaltrialsgov

01

Visit the clinicaltrials.gov website

02

Create a user account if you don't already have one

03

Click on the 'Submit Studies' tab

04

Enter the required information for your clinical trial, such as study title, protocol ID, and study design

05

Upload any relevant documents, such as the study protocol or informed consent form

06

Review and submit your study for review

Who needs classic clinicaltrialsgov?

01

Researchers conducting clinical trials

02

Pharmaceutical companies

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Government agencies

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Healthcare providers

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Medical professionals

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What is classic clinicaltrialsgov?

Classic clinicaltrialsgov is a registry and results database of publicly and privately supported clinical studies of human participants.

Who is required to file classic clinicaltrialsgov?

The responsible party, usually the sponsor or the investigator, is required to file classic clinicaltrialsgov.

How to fill out classic clinicaltrialsgov?

Classic clinicaltrialsgov can be filled out online through the official website by providing information about the study, including protocol details and results.

What is the purpose of classic clinicaltrialsgov?

The purpose of classic clinicaltrialsgov is to provide transparency and access to information about clinical trials for the public and healthcare professionals.

What information must be reported on classic clinicaltrialsgov?

Information such as study protocol details, recruitment status, study results, and adverse event information must be reported on classic clinicaltrialsgov.

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