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Effect of Pulsed Electromagnetic Field Therapy on Pain After Cesarean Delivery

NCT02365753 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 84

Last updated 2019-04-04

No results posted yet for this study

Summary

A double-blinded randomized control study using a pulsed electromagnetic field therapy to establish whether this device decreases patient pain and decreases narcotic use in women who have undergone cesarean delivery.

Conditions

  • Postoperative Pain

Interventions

DEVICE

SofPulse

Pulsed Electomagnetic Field Therapy Device placed over incision and turned on and kept in place with tape.

Sponsors & Collaborators

  • New York City Health and Hospitals Corporation

    lead OTHER

Principal Investigators

  • Donald C Phillibert, MD · Jacobi Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-01-31
Primary Completion
2017-09-17
Completion
2018-10-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02365753 on ClinicalTrials.gov