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Transcutaneous Electrical Nerve Stimulation for Post-Cesarean Pain Control

NCT04399707 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 180

Last updated 2020-05-26

No results posted yet for this study

Summary

Purpose of study is to evaluate the efficacy of transcutaneous electrical nerve stimulation (TENS) for post-operative pain control after a cesarean delivery compared to placebo and no TENS.

Conditions

  • Transcutaneous Electric Nerve Stimulation
  • Analgesia
  • Cesarean Section

Interventions

DEVICE

Transcutaneous electrical nerve stimulation (TENS) unit

Patients will be randomized to active TENS unit, placebo TENS unit, or no TENS unit

DEVICE

Placebo transcutaneous electrical nerve stimulation (TENS) unit

Patients will be randomized to active TENS unit, placebo TENS unit, or no TENS unit

Sponsors & Collaborators

  • Hawaii Pacific Health

    lead OTHER

Principal Investigators

  • Kelly Yamasato · Physician

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-01-29
Primary Completion
2021-05-31
Completion
2021-05-31
FDA Device
Yes

Countries

  • United States

Study Locations

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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 NCT04399707 on ClinicalTrials.gov