At a glance
ClinicalIndex Comparison RecordN/ACompleted· 70 enrolled
Drug / intervention
OrthoPAT +1 moredevice
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.
A Prospective Randomized Study on the Clinical Benefits of OrthoPAT Drains for Adults Undergoing Multilevel Spine Surgery for Deformity
In Brief
A clinical study evaluating OrthoPAT and Constavac for Spine Deformity. Completed, enrolled 70 participants across 1 site.
Detailed Summary
The examination of the ability of the OrthoPAT® blood collection device to decrease the transfusion rate and volume of adults undergoing posterior spine surgery for deformity correction of 6 levels or more.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSpine Deformity
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
Enrollment StartJan 2011
First PostedNov 2014
Primary CompletionAug 2015
Study CompletionOct 2016
TodayJul 2026
First PostedNov 7, 2014
Enrollment StartJan 1, 2011
Primary CompletionAug 1, 2015
Study CompletionOct 17, 2016
TodayJul 2, 2026
Enrollment to primary: 4.6 yearsPosted 11.7 years ago
Interventions
OrthoPATdevice
OrthoPAT drain to collect and retransfuse postoperative blood loss. Drains will be removed 48 hours postoperatively
Constavacdevice
Constavac drain to collect postoperative blood loss. Drains will be removed 48 hours postoperatively