Apply to trial NCT07185425

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RecruitingDevice study

Impact of the NeuroCuple Device on Pain Management After Cesarean Delivery

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.

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Impact of the NeuroCuple Device on Pain Management After Cesarean Delivery

How this works

Answer a few questions

We connect you with the study team

The team reaches out to schedule screening