At a glance
ClinicalIndex Comparison RecordN/ACompleted· 151 enrolled
Drug / intervention
Dermabond Prineo +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.
Glue Versus Subcuticular Suture for Cesarean Closure: a Randomized Control Trial
In Brief
A clinical study evaluating Dermabond Prineo and Suture for Cesarean Section and 2 related conditions. Completed, enrolled 151 participants across 1 site.
Detailed Summary
The aim of this study is to compare cesarean incision outcomes between patients with incision closed with the Dermabond Prineo system compared to standard subcuticular suture.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCesarean Section, Complication, Wound
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
202420252026
First PostedJun 2023
Enrollment StartAug 2023
Primary CompletionDec 2024
Study CompletionFeb 2025
TodayJul 2026
First PostedJun 15, 2023
Enrollment StartAug 23, 2023
Primary CompletionDec 6, 2024
Study CompletionFeb 5, 2025
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 3.0 years ago
Interventions
Dermabond Prineodevice
For subjects in the Dermabond Prineo group, the Dermabond Prineo system will be applied to the skin for skin closure under manufacturer's guidelines.
Sutureother
For subjects in the Suture group, the skin will be closed with the standard subcuticular suture method.