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Acupuncture for post anaesthetic recovery and postoperative pain: study protocol for a randomised controlled trial.

Trials
January 1, 1970
Johannes Fleckenstein et al. (8 authors)
Comparative StudyJournal ArticleRandomized Controlled TrialResearch Support, Non-U.S. Gov'tHuman StudyClinical
Study Details

Study Goal

The researchers aimed to compare the effectiveness of press needle acupuncture, no treatment, and press plaster acupressure on post-anesthetic recovery and postoperative pain in patients undergoing laparoscopic surgery.

Results Summary

The study did not report specific results for acupressure, as it was a pilot trial designed to compare acupuncture and acupressure with no treatment; the primary outcome was time from extubation to readiness for discharge.

Population

75 patients scheduled for laparoscopic surgery to the uterus or ovaries.

Effective Dosage

12 press plasters administered preoperatively at seven acupuncture points.

Duration

The intervention was administered preoperatively, with observation from one day before surgery to the second postoperative day.

Interactions

None mentioned

Extracted Claims (4)
InterventionDirectionEndpointPopulationDosageImpactClaim #
press needle acupuncture
neutral
post anaesthetic recovery
patients scheduled for laparoscopic surgery to the uterus or ovaries
-
investigate the effectiveness
#1
press needle acupuncture
neutral
postoperative pain
patients scheduled for laparoscopic surgery to the uterus or ovaries
-
investigate the effectiveness
#2
acupuncture
increase
patient post anaesthetic recovery
-
-
may improve
#3
acupuncture
neutral
therapeutic differences between invasive and non-invasive acupuncture techniques
-
-
comparing with acupressure will provide insight into potential therapeutic differences
#4
Abstract

BACKGROUND: We report on the design and implementation of a study protocol entitled Acupuncture randomised trial for post anaesthetic recovery and postoperative pain - a pilot study (ACUARP) designed to investigate the effectiveness of acupuncture therapy performed in the perioperative period on post anaesthetic recovery and postoperative pain. METHODS/DESIGN: The study is designed as a randomised controlled pilot trial with three arms and partial double blinding. We will compare (a) press needle acupuncture, (b) no treatment and (c) press plaster acupressure in a standardised anaesthetic setting. Seventy-five patients scheduled for laparoscopic surgery to the uterus or ovaries will be allocated randomly to one of the three trial arms. The total observation period will begin one day before surgery and end on the second postoperative day. Twelve press needles and press plasters are to be administered preoperatively at seven acupuncture points. The primary outcome measure will be time from extubation to 'ready for discharge' from the post anaesthesia care unit (in minutes). The 'ready for discharge' end point will be assessed using three different scores: the Aldrete score, the Post Anaesthetic Discharge Scoring System and an In-House score. Secondary outcome measures will comprise pre-, intra- and postoperative variables (which are anxiety, pain, nausea and vomiting, concomitant medication). DISCUSSION: The results of this study will provide information on whether acupuncture may improve patient post anaesthetic recovery. Comparing acupuncture with acupressure will provide insight into potential therapeutic differences between invasive and non-invasive acupuncture techniques. TRIAL REGISTRATION: NCT01816386 (First received: 28 October 2012).

Medical Subject Headings (MeSH)
AcupressureAcupuncture AnalgesiaAcupuncture PointsAnesthesia Recovery PeriodClinical ProtocolsDouble-Blind MethodFemaleGermanyGynecologic Surgical ProceduresHumansLaparoscopyPain MeasurementPain, PostoperativePilot ProjectsPostoperative CareResearch DesignTime FactorsTreatment Outcome
Study Links
Quality Scores
SafetyNot Assessed
Efficacy65/10
Quality80/10
Citation Metrics
Total Citations13
Citations/Year1.2
Relative Citation Ratio0.75
NIH Percentile39.8%
Research Impact Scores
APT Score0.50
Weight Score1.69
Normalized Score0.62
Related Supplements
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