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NCT07185425 · ClinicalTrials.gov registry record · NA
Impact of the NeuroCuple Device on Pain Management After Cesarean Delivery
A NA study of Pain and Pregnancy, sponsored by Inova Health Care Services.
- Recruiting
- Registry status
- NA
- Development phase
- 180
- Enrollment target
- 1
- Study location
NCT07185425 is a NA study of Pain and Pregnancy that is actively recruiting participants, run by Inova Health Care Services. The registered enrollment target is 180 participants, below the 304-participant average among 374 other Pain trials with a reported enrollment target (41% lower). The trial reports 1 study location across 1 state.
The verdict
NCT07185425, a NA study of Pain and Pregnancy, is actively recruiting participants, sponsored by Inova Health Care Services.
- RECRUITING
- Registry status
- NA
- Development phase
- 180 participants
- Enrollment target
- 1
- Study location
Study 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.
Interventions
- DEVICE Sham
- DEVICE NeuroCuple
Study Locations (1)
Virginia
- Inova Fairfax Medical Campus - Falls Church
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 180 participants |
| Start Date | 2025-10-13 |
| Est. Completion | 2027-09 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07185425
The ClinicalTrials.gov registry entry for NCT07185425 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 180 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 304-participant average among 374 other Pain trials with a reported enrollment target (41% lower). The listed sponsor is Inova Health Care Services, which has 75 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Pain appearing as the primary indexed condition, and to 2 interventions - of which Sham is the first listed.
NCT07185425 reports 1 study location spanning 1 distinct geographic area - top geographies include Virginia.
Frequently Asked Questions
What is clinical trial NCT07185425 about?
NCT07185425 is a clinical study titled "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 wit...
What is the current status of trial NCT07185425?
This trial is currently recruiting. It is a NA study. The enrollment target is 180 participants. The study started on 2025-10-13. Estimated completion is 2027-09.
What conditions does trial NCT07185425 study?
This clinical trial studies the following conditions: Pain, Pregnancy, Analgesia.
What interventions are being tested in trial NCT07185425?
The interventions under investigation include: Sham (DEVICE), NeuroCuple (DEVICE).
Who is sponsoring clinical trial NCT07185425?
This trial is sponsored by Inova Health Care Services, which has 75 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07185425 being conducted?
This trial has 1 study location across Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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