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NCT02368379 · ClinicalTrials.gov registry record · NA

Diagnosis of Central Adrenal Insufficiency in Patients With Prader-Willi Syndrome

A NA study, sponsored by Nationwide Children's Hospital.

Completed
Registry status
NA
Development phase
23
Enrollment target

NCT02368379: Completed NA study, sponsored by Nationwide Children's Hospital.

NCT02368379 is a NA study that has completed, run by Nationwide Children's Hospital. The registered enrollment target is 23 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02368379, a NA study, has completed, sponsored by Nationwide Children's Hospital.

COMPLETED
Registry status
NA
Development phase
23 participants
Enrollment target

Study Summary

The purpose of this study is to determine presence of central adrenal insufficiency in children with Prader Willi Syndrome using low dose (1 mcg) ACTH stimulation test compared to results of overnight metyrapone test.

Interventions

  • OTHER Low dose (1 mcg) ACTH stimulation test
  • OTHER Overnight metyrapone test

Trial Details

FieldValue
Enrollment Target 23 participants
Start Date 2014-03
Est. Completion 2016-08
Phase NA
Nationwide Children's Hospital

188 total trials

What the finished NCT02368379 record still lists

NCT02368379 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 23 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 2 interventions - of which Low dose (1 mcg) ACTH stimulation test is the first listed.

NCT02368379 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02368379 about?

NCT02368379 is a clinical study titled "Diagnosis of Central Adrenal Insufficiency in Patients With Prader-Willi Syndrome". The purpose of this study is to determine presence of central adrenal insufficiency in children with Prader Willi Syndrome using low dose (1 mcg) ACTH stimulation test compared to results of overnight metyrapone test.

What is the current status of trial NCT02368379?

This trial is currently completed. It is a NA study. The enrollment target is 23 participants. The study started on 2014-03. Estimated completion is 2016-08.

What interventions are being tested in trial NCT02368379?

The interventions under investigation include: Low dose (1 mcg) ACTH stimulation test (OTHER), Overnight metyrapone test (OTHER).

Who is sponsoring clinical trial NCT02368379?

This trial is sponsored by Nationwide Children's Hospital, which has 188 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02368379's enrollment target sits among peer trials

23 1755th of 2000 higher than 245 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02368379, the US trial registry maintained by the National Library of Medicine. NCT02368379 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.