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The Effect of Traxi Panniculus Retractor on Surgical Time at Non-emergent Cesarean Delivery in Obese Women

Obesity Clinical Trial

Official title:
The Effect of Traxi Panniculus Retractor on Surgical Time at Non-emergent Cesarean Delivery in Obese Women

Clinical Trial Summary

This is an unblinded, randomized control trial of obese women to evaluate the impact of the Traxi Panniculus Retractor (TPR) on the cesarean operative time and surgical blood loss when compared to silk tape.

Clinical Trial Description

The purpose of the study is to assess whether using the Traxi Panniculus Retractor during cesarean section, in obese (BMI greater than or equal to 30kg/m2 at time of delivery) women, can decrease the cesarean operative time compared to using silk tape to retract the panniculus. Operative time is defined as the time from when the patient lies on the operating room table (at completion of the epidural/spinal anesthesia) until fascial closure. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04458415
Study type Interventional
Source Geisinger Clinic
Contact
Status Withdrawn
Phase N/A
Start date June 1, 2021
Completion date April 30, 2022
View Details
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