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The Effect of Acupuncture on the Management of Postoperative pain control in total knee arthroplasty.

Not Applicable
Recruiting
Conditions
Surgery
post operative pain
Registration Number
PACTR201705002261398
Lead Sponsor
Kassab orthopedic institute
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
88
Inclusion Criteria

Patients scheduled for primary total knee arthroplasty under spinal anesthesia.

Exclusion Criteria

¿Contraindication to EA (severe cardiac arrhythmia, seizure disorder, history of psychiatric disease or drug abuse.)
¿Acupuncture treatment within 1 month before the trial.
¿Refusal of acupuncture.
¿Difficulty of communication (deaf patients, demented patients, patients with psychological disorders¿)
¿Contraindication to antiinflammatory drug (patients with ulcer or gastritis, renal failure¿)
¿Allergy to any of the study medications.
¿Contraindication to the realization of spinal anesthesia or refusal of spinal anesthesia.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
the morphine consumption during the first 48 hours.
Secondary Outcome Measures
NameTimeMethod
The time to the first PCA request.;Numerical rating scale pain scores. ;Mobilization ability.;The incidence of analgesia-related adverse effects.;Length of hospital stay (days).;Chronic pain.
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