Impact of the NeuroCuple Device on Pain Management After Cesarean Delivery
Recruiting
N/A
Interventional Study
Pain
Analgesia
Pregnancy
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 180 (estimated)
- Sponsor
- Inova Health Care Services · Other
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About This Trial
This will be a single-center, sham-controlled, 3 arms, randomized (1:1:1) prospective study in females undergoing cesarean delivery to investigate the impact of NeuroCuple™ non-pharmacological analgesic device for management of postoperative pain. The investigators hypothesize that women treated with the Neurocuple device will experience less pain and consequently require less opioid pain medicati…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Female 18 years or older able to provide informed consent in English or Spanish
* Scheduled for a planned or unplanned non-emergent cesarean delivery under neuraxial anesthesia
* Intact skin surfaces around the operative skin incision area at the site of patch application
* Pf…
Contacts