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NCT02586103 · ClinicalTrials.gov registry record
Prospective Study Assessing the Validity of Y-PAS (Yale Preoperative Anxiety Scale) to Predict Patients Undergoing Magnetic Resonance Imaging Without the Use of Sedation/General Anesthesia
A clinical trial, sponsored by Arlyne Thung.
- Completed
- Registry status
- 80
- Enrollment target
NCT02586103 is a clinical trial that has completed, run by Arlyne Thung. The registered enrollment target is 80 participants.
The verdict
NCT02586103 has completed, sponsored by Arlyne Thung.
- COMPLETED
- Registry status
- 80 participants
- Enrollment target
Study Summary
The mYPAS (Modified Yale Preoperative Anxiety Scale) is a quick, easy, validated and "gold standard" assessment tool to measure pediatric anxiety in the perioperative period. Therefore the objective of the current prospective study is examine if the mY-PAS is an effective screening tool to differentiate patients who would succeed versus fail for MRI without sedation/anesthesia.
Interventions
- DEVICE MRI simulation
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2015-11 |
| Est. Completion | 2017-04 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02586103
The ClinicalTrials.gov registry entry for NCT02586103 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Arlyne Thung, which has 4 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which MRI simulation is the first listed.
NCT02586103 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02586103 about?
NCT02586103 is a clinical study titled "Prospective Study Assessing the Validity of Y-PAS (Yale Preoperative Anxiety Scale) to Predict Patients Undergoing Magnetic Resonance Imaging Without the Use of Sedation/General Anesthesia". The mYPAS (Modified Yale Preoperative Anxiety Scale) is a quick, easy, validated and "gold standard" assessment tool to measure pediatric anxiety in the perioperative period. Therefore the objective of the current prospective study is examine if the mY-PAS is an effective screening tool to different...
What is the current status of trial NCT02586103?
This trial is currently completed. The enrollment target is 80 participants. The study started on 2015-11. Estimated completion is 2017-04.
What interventions are being tested in trial NCT02586103?
The interventions under investigation include: MRI simulation (DEVICE).
Who is sponsoring clinical trial NCT02586103?
This trial is sponsored by Arlyne Thung, which has 4 total clinical trials registered on ClinicalTrials.gov.
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