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NCT03973840 · ClinicalTrials.gov registry record · Phase 1

Assessment of Blood From Men Receiving Oral TU in Various Collection Tubes

A Phase 1 study of Hypogonadism, Male, sponsored by Clarus Therapeutics.

Completed
Registry status
Phase 1
Development phase
13
Enrollment target
1
Study location

NCT03973840 is a Phase 1 study of Hypogonadism, Male that has completed, run by Clarus Therapeutics. The registered enrollment target is 13 participants, below the 111-participant average among 12 other Hypogonadism, Male trials with a reported enrollment target (88% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03973840, a Phase 1 study of Hypogonadism, Male, has completed, sponsored by Clarus Therapeutics.

COMPLETED
Registry status
Phase 1
Development phase
13 participants
Enrollment target
1
Study location

Study Summary

To describe the rate of post-collection TU to testosterone conversion, as manifested by increases in testosterone concentration, in Plain tubes held at room temperature and sodium fluoride (NaF)-ethylenediaminetetraacetic acid (EDTA) tubes held at room temperature or on ice prior to centrifugation

Conditions Studied

Interventions

  • DRUG Testosterone Undecanoate

Study Locations (1)

Illinois

  • Clarus Therapeutics, Inc - Northbrook

Trial Details

FieldValue
Enrollment Target 13 participants
Start Date 2018-07-15
Est. Completion 2018-07-31
Phase Phase 1

Sponsor

Clarus Therapeutics

11 total trials

What the Registry Record Tells You About NCT03973840

The ClinicalTrials.gov registry entry for NCT03973840 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 13 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 111-participant average among 12 other Hypogonadism, Male trials with a reported enrollment target (88% lower). The listed sponsor is Clarus Therapeutics, which has 11 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Hypogonadism, Male appearing as the primary indexed condition, and to 1 intervention - of which Testosterone Undecanoate is the first listed.

NCT03973840 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.

Frequently Asked Questions

What is clinical trial NCT03973840 about?

NCT03973840 is a clinical study titled "Assessment of Blood From Men Receiving Oral TU in Various Collection Tubes". To describe the rate of post-collection TU to testosterone conversion, as manifested by increases in testosterone concentration, in Plain tubes held at room temperature and sodium fluoride (NaF)-ethylenediaminetetraacetic acid (EDTA) tubes held at room temperature or on ice prior to centrifugation

What is the current status of trial NCT03973840?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 13 participants. The study started on 2018-07-15. Estimated completion is 2018-07-31.

What conditions does trial NCT03973840 study?

This clinical trial studies the following conditions: Hypogonadism, Male.

What interventions are being tested in trial NCT03973840?

The interventions under investigation include: Testosterone Undecanoate (DRUG).

Who is sponsoring clinical trial NCT03973840?

This trial is sponsored by Clarus Therapeutics, which has 11 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03973840 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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