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Effect of Modulation of TENS in Pain After Cesarean Section

NCT01897311 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 34

Last updated 2017-04-21

No results posted yet for this study

Summary

The aim of the study was to evaluate the analgesic effect of transcutaneous electrical nerve stimulation High (100 Hz) and low (4 Hz) frequency in postpartum pain after cesarean section.

Conditions

Interventions

DEVICE

transcutaneous electrical nerve stimulation

Sponsors & Collaborators

  • Universidade Federal do Piauí

    lead OTHER

Principal Investigators

  • Janaina Mayer de Oliveira Nunes · University Federal Piauí

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
42 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-08-31
Primary Completion
2012-05-31
Completion
2012-08-31

Countries

  • Brazil

Study Locations

More Related Trials

Entities

Diseases

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 NCT01897311 on ClinicalTrials.gov