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Clinical Trials in Germany / NCT04134702
Recruiting Not applicable

Acupuncture for Pain Control After Ambulatory Knee Arthroscopy

NCT04134702 · tracked via the Priya Life Science Germany tracker
Phase
Not applicable
Started
2019-02-01
Last updated
2026-06-09

Condition(s) studied

Postoperative Pain; Knee Arthroscopy; Acupuncture

Investigational drug(s) / intervention(s)

Acupuncture

Acupuncture: Acupuncture and ear acupuncture using indwelling fixed needles, that will remained in situ several days after surgery until the patients will experience pain

Study summary

Aim of the study: To investigate whether acupuncture with indwelling fixed needles reduces pain and analgesic requirement and foster mobilization in patients after arthroscopic knee surgery (AKS) Design: Prospective pilot investigation with non-randomized arm Number of patients: N = 60 (30 patients with acupuncture additional to standard pain treatment (SPT) vs. 30 patients with SPT only Inclusion criteria: Adult patients scheduled to elective AKS in general anaesthesia with \< 80 min. duration Without previous opioid and psychotropic medication Given informed consentOutcome measures: Postoperative analgesic requirement; Pain intensity; Incidence of side effects; Physiological parameters; Mobilization score

Eligibility

Sex
ALL
Min age
19 Years
Max age
55 Years
Healthy volunteers
Accepted
Inclusion Criteria: 1. Patients with an American Society of Anesthesiologists physical status of I to II scheduled for elective ambulatory arthroscopic knee surgery under standardized general anesthesia 2. Surgery time does not exceed 80 minutes 3. Patients without previous opioid and psychotropic medication 4. Patients aged between 19 and 55 years, able to fill in the study questionnaire (Appendix F) 5. Patients who have given written informed consent Exclusion Criteria: 1. Current psychiatric disease 2. Local skin infection at the sites of acupuncture 3. Aged \< 19 or \> 55 years 4. Failure to follow the standardized schema of general anaesthesia 5. Surgery time more than 80 minutes 6. Intraoperative complications (bleeding, required blood transfusion more than 6 units of packed cells, cardiovascular instability, required catecholamines) 7. Patients who consumed opioid medication at least 6 months before surgery 8. Patients who are unable to understand the consent form or to fill in the study questionnaire.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University Medicine of Greifswald Greifswald Vorpommern Recruiting

More University Medicine Greifswald trials in Germany

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04134702 on ClinicalTrials.gov ↗ ← All trials in Germany