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Recruiting NCT07185425

Impact of the NeuroCuple Device on Pain Management After Cesarean Delivery

No phase Interventional Pain Analgesia Pregnancy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: NeuroCuple, Sham.
Who it may be relevant to
Registry conditions: Pain, Analgesia, Pregnancy. Basic parameters: from 18 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

Management of Postoperative Pain After Cesarean Delivery Using Non-pharmacological Analgesic Device, NeuroCuple™

Overview

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.

Detailed description

This is a single-center, sham-controlled, 3-arms, randomized, prospective study in 180 women undergoing cesarean delivery, with an expected subject enrollment duration of one year. Subjects will be screened and consented preoperatively before the scheduled case. Enrolled subjects will be randomized by research personnel using a computer generated randomization scheme in a 1:1:1 group allocation and assigned to the active device, sham device, or standard of care arms.

Upon arrival to the PACU, subjects in the standard-of-care arm will receive standard postoperative pain orders at the discretion of the primary OB/GYN. For subjects in the active and sham device arms, device will be placed as soon as feasible in the PACU and before transfer to the post-partum floor by trained research staff. Both patients and the clinical team will be blinded to the group assignment for the active and sham devices.

Pain scores will be collected from the study participants per nursing protocols while inpatient, and daily after discharge until postoperative day 4, using the Pain Numeric Rating Scale. For breakthrough pain, patients may use oral or IV opioids in the inpatient setting and oral opioids in the outpatient setting.

Upon discharge, patients are typically prescribed an opioid medication. However, this will also be left to the discretion of the primary OB/GYN. In this study, the investigators will examine total milligram morphine equivalent (MME) opioid intake at postoperative day 4 or before discharge as the primary endpoint, reduction (percentage change) in numeric pain scale as the secondary endpoint, and change in quality of recovery as the exploratory endpoint.

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

Primary outcome measures

  • Total Milligram Morphine Equivalents (MME) [Time frame: Day of surgery to postop day 4]
Secondary outcome measures (3)
  • Pain reduction [Time frame: Day of surgery to postop day 4]
  • Quality of Recovery [Time frame: Day of surgery to postop day 4]
  • Opioid-related adverse events [Time frame: Day of surgery to postop day 4]

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
  • Pfannestiel skin incision

Exclusion criteria

  • Active drug abuse
  • Chronic opioid user
  • Severe chronic pain
  • Psoriasis vulgaris or other skin conditions precluding safe device application
  • Subject is concurrently participating in another research study with an investigational drug or medical device that in the Investigator's opinion could impact subject safety or study results
  • Subject with reasons to maintain an epidural beyond operative room
  • Subject with complex surgery or subject who may need more than a cesarean surgery with possible tubal sterilization procedure
  • Subject is deemed not suitable for the study at the discretion of the principal Investigator

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Quadruple blind
Primary purpose
Treatment

Study locations

United States · 1 center
  • Inova Fairfax Medical Campus — Falls Church

Identifiers

NCT: NCT07185425 · INOVA-2025-16

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗