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Postoperative Analgesia After Low Frequency Electroacupuncture

NCT01722253 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 54

Last updated 2015-06-08

No results posted yet for this study

Summary

The purpose of this study is to determine whether electroacupuncture is a effective tool to the postoperative analgesia

Conditions

  • Inguinal Hernia

Interventions

PROCEDURE

Electroacupuncture

Electrical stimulation device with frequency 2 Hz and 'frequency scanning mode'

Sponsors & Collaborators

  • Aristotle University Of Thessaloniki

    lead OTHER

Principal Investigators

  • Dimitrios G Vasilakos, Professor · Aristotle University

  • Maria I Dalamagka, consultant · Aristotle University

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-12-31
Primary Completion
2015-03-31
Completion
2015-04-30

Countries

  • Greece

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 NCT01722253 on ClinicalTrials.gov