At a glance
ClinicalIndex Comparison RecordN/ACompleted· 10 enrolled
Drug / intervention
InPress Devicedevice
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.
Feasibility Clinical Investigation Using the InPress Device for the Treatment of Postpartum Hemorrhage
In Brief
A clinical study evaluating InPress Device for Post Partum Hemorrhage. Completed, enrolled 10 participants across 2 sites.
Detailed Summary
Feasibility trial of the InPress Device to treat postpartum hemorrhage (PPH).
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPost Partum Hemorrhage
CountriesIndonesia
Collaborators--
Timeline
N/ACompletedFinished
201520162017201820192020202120222023202420252026
Enrollment StartJul 2014
Primary CompletionFeb 2015
Study CompletionApr 2015
First PostedApr 2020
TodayJul 2026
First PostedApr 28, 2020
Enrollment StartJul 27, 2014
Primary CompletionFeb 11, 2015
Study CompletionApr 1, 2015
TodayJul 2, 2026
Enrollment to primary: 6 monthsPosted 6.2 years ago
Interventions
InPress Devicedevice
Treatment with InPress Device for Postpartum Hemorrhage