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N/A Completed N=42 Randomized Treatment

Evaluating Transcutaneous Electrical Nerve Stimulation for Postoperative Pain After Video-Assisted Thoracotomy Surgery

Source: ClinicalTrials.gov NCT01046695 ↗
Enrolled (actual)
42
Serious AEs
0.0%
Results posted
Dec 2012
Primary outcomePrimary: Mean Pain Score — 4.55; 3.85; 4.30; 3.80 units on a scale

Summary

We propose to evaluate the use of Transcutaneous Electrical Nerve Stimulation (TENS) in patients having undergone Video-Assisted Thoracotomy Surgery (VATS) with the aim to determine if: * Nurses will be able to apply TENS effectively and in a timely manner to post VATS patients. * Use of TENS immediately after thoracic surgery and for the first 48 hours will add to patient's pain control. * Tens will reduce medication use. * Tens will reduce nausea and vomiting.

Outcome Measures

OutcomeResultp-value
PRIMARY
Mean Pain Score
4.55; 3.85; 4.30; 3.80; 4.30; 3.95
SECONDARY
Mean Opioid Use, Converted Into Oral Morphine Equivalents (OME) at 24 and 48 Hours
90.19; 93.65; 47.50; 69.68 .005 sig
SECONDARY
Satisfaction With Pain Control at 48 Hours
2; 2; 1; 2; 0; 2 .70

Eligibility Criteria

Inclusion Criteria

  • Men and women age 18-100 able to give informed consent.
  • Able to speak and understand English.

Exclusion Criteria

  • Too confused to provide data or not extubated within 48 hours after surgery.
  • Unable to speak and understand English.
  • Patients with active internal pacer wires, demand type implanted pacemakers or defibrillator.
  • Transplant patients.
  • Children, prisoners, any woman who is pregnant.
  • Patients that are non-scheduled surgery cases or occurring Saturday or Sunday.
  • Ventricular Assisted Device (VAD) patients.
  • Know allergies or intolerance to TENS electrodes.
  • Patients who have had the Da Vinci robotic assisted minimally invasive procedure.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01046695). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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