Neuromuscular Electrical Stimulation Following Total Hip Arthroplasty

NCT01785251 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 11

Last updated 2013-02-07

No results posted yet for this study

Summary

Patients post total hip arthroplasty (THA) remain at high risk of developing Deep Vein Thrombosis (DVT) during the recovery period following surgery despite the availability of effective pharmacological and mechanical prophylactic methods. The use of calf muscle neuromuscular electrical stimulation (NMES) during the hospitalised recovery period on this patient group may be effective at preventing DVT. However, the haemodynamic effectiveness and comfort characteristics of NMES in post-THA patients immediately following surgery have yet to be established.

The main objectives are:

1. To establish if patients in the early post-operative period have tolerance for NMES.
2. To determine if applying NMES to patients immediately post-THA increases venous outflow from the lower limb over resting conditions.

Conditions

  • Deep Vein Thrombosis
  • Total Hip Arthroplasty

Interventions

DEVICE

Neuromuscular Electrical Stimulation

Applied using a custom built, medically approved stimulator called the Duo-STIM. NMES to be applied to the calf muscles to elicit a muscular contraction to eject blood through the venous system.

Sponsors & Collaborators

  • Irish Research Council

    collaborator OTHER
  • Mid Western Regional Hospital, Ireland

    collaborator OTHER
  • National University of Ireland, Galway, Ireland

    lead OTHER

Principal Investigators

  • Gearóid ÓLaighin, BEng, MEng, PhD · National University of Ireland, Galway

Study Design

Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
30 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-06-30
Primary Completion
2012-02-29
Completion
2012-02-29

Countries

  • Ireland

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 NCT01785251 on ClinicalTrials.gov