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NCT03695900 · ClinicalTrials.gov registry record · NA

Arterial Oxygen Saturation on Ventilatory Stability in Extremely Premature Infants

A NA study of Apnea of Prematurity and Desaturation of Blood, sponsored by University of Miami.

Completed
Registry status
NA
Development phase
19
Enrollment target
1
Study location

NCT03695900: Completed NA study of Apnea of Prematurity and Desaturation of Blood, sponsored by University of Miami.

NCT03695900 is a NA study of Apnea of Prematurity and Desaturation of Blood that has completed, run by University of Miami. The registered enrollment target is 19 participants, below the 406-participant average among 6 other Apnea of Prematurity trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03695900, a NA study of Apnea of Prematurity and Desaturation of Blood, has completed, sponsored by University of Miami.

COMPLETED
Registry status
NA
Development phase
19 participants
Enrollment target
1
Study location

Study Summary

This is a prospective crossover study to compare the within-subject effect of the two target ranges of arterial oxygen saturation (SpO2), both within the clinically recommended range of 90- 95%. The specific objective of this study to evaluate the impact of targeting SpO2 within 93-95% compared to the 90-92% range on ventilatory stability in premature infants of 23-29 weeks gestational age (GA).

Primary Outcome

by frequency of central apnea

Interventions

  • OTHER Targeting SpO2 at 93-95%
  • OTHER Targeting SpO2 at 90-92%

Study Locations (1)

Florida

  • Holtz Children's Hospital - Miami

Trial Details

FieldValue
Enrollment Target 19 participants
Start Date 2018-11-01
Est. Completion 2019-11-08
Phase NA
University of Miami

721 total trials

What the finished NCT03695900 record still lists

NCT03695900 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 19 participants, a relatively small participant target, below the 406-participant average among 6 other Apnea of Prematurity trials with a reported enrollment target (95% lower).

The record links to 5 conditions, with Apnea of Prematurity appearing as the primary indexed condition, and to 2 interventions - of which Targeting SpO2 at 93-95% is the first listed.

NCT03695900 reports a single indexed study location in Florida.

Frequently Asked Questions

What is clinical trial NCT03695900 about?

NCT03695900 is a clinical study titled "Arterial Oxygen Saturation on Ventilatory Stability in Extremely Premature Infants". This is a prospective crossover study to compare the within-subject effect of the two target ranges of arterial oxygen saturation (SpO2), both within the clinically recommended range of 90- 95%. The specific objective of this study to evaluate the impact of targeting SpO2 within 93-95% compared to t...

What is the current status of trial NCT03695900?

This trial is currently completed. It is a NA study. The enrollment target is 19 participants. The study started on 2018-11-01. Estimated completion is 2019-11-08.

What conditions does trial NCT03695900 study?

This clinical trial studies the following conditions: Apnea of Prematurity, Desaturation of Blood, Central Apnea, Periodic Breathing, Obstructive Apnea of Newborn.

What interventions are being tested in trial NCT03695900?

The interventions under investigation include: Targeting SpO2 at 93-95% (OTHER), Targeting SpO2 at 90-92% (OTHER).

Who is sponsoring clinical trial NCT03695900?

This trial is sponsored by University of Miami, which has 721 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03695900 being conducted?

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

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Source: ClinicalTrials.gov NCT03695900, the US trial registry maintained by the National Library of Medicine. NCT03695900 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.