Post-Op Lidocaine Patch

Completed · Phase 4 · Has a placebo group

Conditions studied: Pain, Postoperative

In brief

Randomized control trial evaluating use of lidocaine vs placebo patch for post-operative cesarean incision pain.

Key facts

Study ID

NCT03500211

Run by

Oregon Health and Science University

People needed

50

Starts

2018-03-13

Expected to finish

2019-03-01

Last updated by the study team

2020-03-11

Who can join

Age: 18 and older, up to 89. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Pregnant patients who require a scheduled or non-urgent cesarean birth
• Patient able to receive neuraxial analgesia
• Patient able to give verbal and written consent for both cesarean birth and study

You may not qualify if…

• Patients requiring emergent cesarean birth
• Patients allergic to lidocaine or adhesive
• Patients who have already received an epidural during this admission or requiring general anesthesia for cesarean birth
• Patients using chronic oral neuromodulators
• Patients with cardiac disease or using anti-arrhythmic agents
• Patients with fibromyalgia or chronic pain syndromes such as rheumatoid arthritis, osteoarthritis, or lupus.
• Daily narcotic or opiate use for greater than the 2 months prior to enrollment in the study.

Where it is running

• Oregon Health and Science University — Portland, Oregon, United States

Full record on ClinicalTrials.gov

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