At a glance
ClinicalIndex Comparison RecordN/ACompleted· 35 enrolled
Drug / intervention
8mm port +1 moreprocedure
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.
Port Size and Post-Operative Pain Perception by Patients
In Brief
A clinical study evaluating 8mm port and 12mm port for Pain. Completed, enrolled 35 participants across 1 site.
Detailed Summary
The purpose of this study is to determine if there is a difference in pain perception by participants when the assistant port size varies by 50% (8 mm to 12 mm).
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPain
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
Enrollment StartAug 2015
First PostedAug 2015
Primary CompletionNov 2017
TodayJul 2026
First PostedAug 13, 2015
Enrollment StartAug 1, 2015
Primary CompletionNov 16, 2017
TodayJul 2, 2026
Enrollment to primary: 2.3 yearsPosted 10.9 years ago
Interventions
8mm portprocedure
Participate in this arm will have their procedure performed with an 8mm laparoscopic port.
12mm portprocedure
Participate in this arm will have their procedure performed with a 12mm laparoscopic port.