Management of Postoperative Pain With Preemptive Analgesia in Cesarean Section

Status unconfirmed · Not applicable · Has a placebo group

Conditions studied: Labor Pain

In brief

This research will explore the question of whether preincisional skin infiltration with bupivacaine 0.25% decreases postoperative pain after Cesarean delivery.

Key facts

Study ID

NCT02879435

Run by

Mark Kosanovich

People needed

120

Starts

2016-06-01

Expected to finish

2017-03-01

Last updated by the study team

2016-08-25

Who can join

Age: 18 and older, up to 45. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• adult pregnant women to age 45 with scheduled cesarean sections at Mercy Hospital and Medical Center

You may not qualify if…

• Emergent cesarean sections and subjects with contraindications to bupivacaine

Where it is running

• Mercy Hospital & Medical Center — Chicago, Illinois, United States (enrolling)

Full record on ClinicalTrials.gov

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