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NCT02250820 · ClinicalTrials.gov registry record · Phase 1
A Comparison of Two Sedation Techniques in Children Undergoing Transthoracic Echocardiography (TTE)
A Phase 1 study of Heart Disease, sponsored by Children's Hospital Medical Center, Cincinnati.
- Completed
- Registry status
- Phase 1
- Development phase
- 280
- Enrollment target
- 1
- Study location
NCT02250820 is a Phase 1 study of Heart Disease that has completed, run by Children's Hospital Medical Center, Cincinnati. The registered enrollment target is 280 participants, below the 2,037-participant average among 31 other Heart Disease trials with a reported enrollment target (86% lower). The trial reports 1 study location across 1 state.
The verdict
NCT02250820, a Phase 1 study of Heart Disease, has completed, sponsored by Children's Hospital Medical Center, Cincinnati.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 280 participants
- Enrollment target
- 1
- Study location
Study Summary
The study will examine the quality of two sedation techniques (dexmedetomidine and pentobarbital) used for children aged 3 to 24 months who are undergoing a transthoracic echocardiography (TTE).
Conditions Studied
Interventions
- DRUG Dexmedetomidine
- OTHER Oral Placebo
- DRUG Pentobarbital
- OTHER Nasal Placebo
Study Locations (1)
Ohio
- Cincinnati Children's Hospital Medical Center - Cincinnati
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 280 participants |
| Start Date | 2014-11 |
| Est. Completion | 2017-12 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02250820
The ClinicalTrials.gov registry entry for NCT02250820 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 280 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,037-participant average among 31 other Heart Disease trials with a reported enrollment target (86% lower). The listed sponsor is Children's Hospital Medical Center, Cincinnati, which has 571 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Heart Disease appearing as the primary indexed condition, and to 4 interventions - of which Dexmedetomidine is the first listed.
NCT02250820 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.
Frequently Asked Questions
What is clinical trial NCT02250820 about?
NCT02250820 is a clinical study titled "A Comparison of Two Sedation Techniques in Children Undergoing Transthoracic Echocardiography (TTE)". The study will examine the quality of two sedation techniques (dexmedetomidine and pentobarbital) used for children aged 3 to 24 months who are undergoing a transthoracic echocardiography (TTE).
What is the current status of trial NCT02250820?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 280 participants. The study started on 2014-11. Estimated completion is 2017-12.
What conditions does trial NCT02250820 study?
This clinical trial studies the following conditions: Heart Disease.
What interventions are being tested in trial NCT02250820?
The interventions under investigation include: Dexmedetomidine (DRUG), Oral Placebo (OTHER), Pentobarbital (DRUG), Nasal Placebo (OTHER).
Who is sponsoring clinical trial NCT02250820?
This trial is sponsored by Children's Hospital Medical Center, Cincinnati, which has 571 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02250820 being conducted?
This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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