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A Randomized Controlled Study on Acupuncture for Periostoperative Pain after Open Radical Prostatectomy

Not Applicable
Conditions
C61
Malignant neoplasm of prostate
Registration Number
DRKS00019884
Lead Sponsor
Martini-Klinik am UKE GmbH
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Male
Target Recruitment
126
Inclusion Criteria

Diagnosis with prostate cancer and scheduled for open radical prostatectomy

Exclusion Criteria

•Inability to understand the terms of this study
•Simultaenous participaton in other clinical trials possibly influencing primary or second-ary end-points or any acupuncture-related clinical trials within 30 days prior to inclusion
•Prior surgery within the last three months
•Received acupuncture within 6 weeks before surgery
•Known hypersensitivity or fear of acupuncture
•Known abuse of drugs, medications and alcohol
•Chronic pain for more than 3 months
•Continuous opioid analgesic medications for more than 3 days during the 4 weeks prior to surgery

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Postoperative pain intensity measured by Numeric Rating Scale (NRS-11) calculated as area under the curve (AUC)
Secondary Outcome Measures
NameTimeMethod
•Cumulative use (sum in mg) of routine postoperative analgesics <br>•Time to first defecation following surgery<br>•EQ-5D-5L for quality of life
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