Wound Infiltration as Part of an Opioid Free Pain Management Pathway Following Cesarean Delivery

Status unconfirmed · Phase 2 · Has a placebo group

Conditions studied: Pain, Postoperative, Anesthesia, Local, Opioid Use

In brief

This study will investigate the effect of three types of wound infiltration on post Cesarean opioid analgesia consumption when used in conjunction with an opioid free postoperative analgesia pathway.

Key facts

Study ID

NCT03545516

Run by

Richmond University Medical Center

People needed

540

Starts

2018-09-17

Expected to finish

2018-11-01

Last updated by the study team

2018-08-29

Who can join

Age: 18 and older, up to 55. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• All scheduled Cesarean deliveries with intrathecal or epidural anesthesia

You may not qualify if…

• Emergency Cesarean deliveries
• Multifetal gestation
• Subjects <18 years old
• Subjects belonging to a vulnerable population (including subjects with a known opioid addiction, subjects with a history of mental illness and prisoners)
• Cesarean delivery with general anesthesia
• Known allergy or hypersensitivity to any of the study medications
• Subjects that can't comprehend the visual analog scale for quantitative pain assessment

Where it is running

• Richmond University Medical Center — Staten Island, New York, United States

Full record on ClinicalTrials.gov

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