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RECRUITING
NCT07185425
NA

Impact of the NeuroCuple Device on Pain Management After Cesarean Delivery

Sponsor: Inova Health Care Services

View on ClinicalTrials.gov

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

DEVICE

NeuroCuple

Device around the abdomen over c-section bandages in the PACU

DEVICE

Sham

Device around the abdomen over c-section bandages in the PACU

Locations (1)

Inova Fairfax Medical Campus

Falls Church, Virginia, United States