At a glance
ClinicalIndex Comparison RecordN/ACompleted· 300 enrolled
Drug / intervention
Not specified
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.
Accurate Display of Postpartum Hemorrhage Using Triton (ADOPT) - A Retrospective Blinded Cohort Study
In Brief
An observational study for Post-partum Hemorrhage (PPH). Completed, enrolled 300 participants across 1 site.
Detailed Summary
A comparison of reported estimated blood loss with quantified blood loss in all patients whose medical records indicate Triton was used during their vaginal delivery.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsPost-partum Hemorrhage (PPH)
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2017201820192020202120222023202420252026
Enrollment StartJul 2016
First PostedDec 2016
Primary CompletionJul 2018
Study CompletionSep 2019
TodayJul 2026
First PostedDec 5, 2016
Enrollment StartJul 1, 2016
Primary CompletionJul 1, 2018
Study CompletionSep 1, 2019
TodayJul 2, 2026
Enrollment to primary: 2 yearsPosted 9.6 years ago