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Auricular Acupuncture for Analgesia During Total Hip Arthroplasty

Auricular Acupuncture (AA) vs. Sham Acupuncture for Complementary Analgesia During Elective Total Hip Arthroplasty: a Randomized Controlled Trial

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00334165
Enrollment
360
Registered
2006-06-06
Start date
2005-06-30
Completion date
2008-06-30
Last updated
2011-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Pain, Total Hip Arthroplasty

Brief summary

The aim is to investigate whether auricular acupuncture is superior to sham acupuncture in relief of acute pain and in reduction of analgesics in patients during total hip arthroplasty

Interventions

PROCEDUREAuricular acupuncture (procedure)

Sponsors

Humboldt-Universität zu Berlin
CollaboratorOTHER
University Medicine Greifswald
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
45 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

1. Patients with an American Society of Anesthesiologists physical status of I to III scheduled for elective hip arthroplasty because of degenerative osteoarthritis under general anesthesia. 2. Surgery time does not exceed 100 minutes. 3. Patients without previous opioid medication. 4. Patients ranged 45-85 years old. 5. Patients who have given informed consent.

Exclusion criteria

1. Pregnant or nursing females. 2. Recidivist alcoholics. 3. Local or systemic infection. 4. Age \< 45 and \> 85 years. 5. Surgery time more than 100 minutes. 6. Intraoperative complications (bleeding, required blood transfusion more than 4 units of packed cells , cardiovascular instability, required catecholamines). 7. Patients consumed opioid medication before surgery. 8. Patients with prosthetic or damaged cardiac valves. 9. Patients who are unable to understand the consent form. 10. History of psychiatric disease.

Design outcomes

Primary

MeasureTime frame
Intraoperative analgesics requirement

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026