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Port Size and Post-Operative Pain Perception by Patients

NCT02521987 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 35

Last updated 2018-02-01

No results posted yet for this study

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).

Conditions

Interventions

PROCEDURE

8mm port

Participate in this arm will have their procedure performed with an 8mm laparoscopic port.

PROCEDURE

12mm port

Participate in this arm will have their procedure performed with a 12mm laparoscopic port.

Sponsors & Collaborators

  • Loyola University

    lead OTHER

Principal Investigators

  • Elizabeth R Mueller, MD · Loyola University Health System

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-08-01
Primary Completion
2017-11-16
Completion
2017-11-16

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02521987 on ClinicalTrials.gov