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Impact of the NeuroCuple Device on Pain Management After Cesarean Delivery
Sponsor: Inova Health Care Services
Summary
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 medication after cesarean delivery compared to women who receive standard post-surgical medication.
Official title: Management of Postoperative Pain After Cesarean Delivery Using Non-pharmacological Analgesic Device, NeuroCuple™
Key Details
Gender
FEMALE
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
180
Start Date
2025-10-13
Completion Date
2027-09
Last Updated
2025-10-16
Healthy Volunteers
No
Interventions
NeuroCuple
Device around the abdomen over c-section bandages in the PACU
Sham
Device around the abdomen over c-section bandages in the PACU
Locations (1)
Inova Fairfax Medical Campus
Falls Church, Virginia, United States