At a glance
ClinicalIndex Comparison RecordN/ACompleted· 77 enrolled
Drug / intervention
CRI device (non-invasive vitals sign measurement)device
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Evaluation of the Compensatory Reserve Index and Psychosocial Factors in Pediatric Autonomic Dysfunction
In Brief
An observational study evaluating CRI device (non-invasive vitals sign measurement) for Postural Orthostatic Tachycardia Syndrome. Completed, enrolled 77 participants across 1 site.
Detailed Summary
The investigators aim to study whether the Compensatory Reserve Index (CRI) (an FDA approved device that assesses intravascular volume) can be used to evaluate severity of Postural Orthostatic Tachycardia Syndrome (POTS) and whether the CRI value has a correlation with severity of psychosocial symptoms and functional impairment associated with POTS.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsColorado Clinical & Translational Sciences Institute
Timeline
N/ACompletedFinished
2020202120222023202420252026
Enrollment StartJun 2019
First PostedJun 2019
Primary CompletionSep 2020
Study CompletionSep 2020
TodayJul 2026
First PostedJun 5, 2019
Enrollment StartJun 1, 2019
Primary CompletionSep 1, 2020
Study CompletionSep 22, 2020
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 7.1 years ago
Interventions
CRI device (non-invasive vitals sign measurement)device
Survey administration, Orthostatic vital measurements