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Clinical Trials/NCT02333747
NCT02333747
Completed
Not Applicable

The Effects of Transcutaneous Electrical Acupoint Stimulation on the Quality of Recovery After Thyroidectomy Surgery

Fujian Provincial Hospital1 site in 1 country84 target enrollmentJanuary 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative Complications
Sponsor
Fujian Provincial Hospital
Enrollment
84
Locations
1
Primary Endpoint
the quality of recovery, as measured by a 40-item questionnaire
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The effect of transcutaneous electric acupoint stimulation (TEAS) on the quality of recovery in patients undergoing thyroidectomy surgery remains unclear. Therefore, the investigators conducted this prospective, randomized, double-blind study to verify the hypothesis that pre-operative TEAS could improve the quality of recovery (QoR) after thyroidectomy surgery.

Detailed Description

Transcutaneous electric acupoint stimulation (TEAS) is a form of non-invasive electrical stimulation that produces a perceptible sensation via electrodes attached to the skin. It has no risk of infections and can potentially be applied by medical personnel with minimal training. Clinical trials have demonstrated that TEAS reduces the consumption of intra-operative anesthetics and general anesthesia related side-effects.

Registry
clinicaltrials.gov
Start Date
January 2015
End Date
May 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Yao Yusheng

Professor

Fujian Provincial Hospital

Eligibility Criteria

Inclusion Criteria

  • Consecutive female patients aged 18 to 60 with American Society of Anesthesiologists physical status (ASA) physical status I or II, who underwent general anesthesia for elective thyroidectomy surgery

Exclusion Criteria

  • potentially difficult airway,
  • a history of chronic pain,
  • drug or alcohol abuse,
  • mental disorder,
  • intake of any analgesic drug within 48 h before surgery, and
  • previous experience with acupuncture treatment

Outcomes

Primary Outcomes

the quality of recovery, as measured by a 40-item questionnaire

Time Frame: 24 hours after surgery

The primary outcome was the quality of recovery, which was assessed on the day before surgery and 24 h after surgery using a 40-item questionnaire (QoR-40)

Secondary Outcomes

  • postoperative pain intensity, as assessed using Visual Analogue Scale (VAS)(24 hours after surgery)
  • the incidence of postoperative nausea and vomiting(24 hours after surgery)
  • patient's satisfaction, as evaluated with a 10-point numerical rating scale: 10= excellent, 1= bad.(at 24 hours after surgery)

Study Sites (1)

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