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Acupuncture vs. Standard Therapy for Treatment of Postoperative Pain in Patients Scheduled for Arthroscopic Knee Surgery - a Pilot Non-randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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
Participation Requirements
Sex: All
Minimum Age: 19
Maximum Age: 55
Healthy Volunteers: t
View:

• Patients with an American Society of Anesthesiologists physical status of I to II scheduled for elective ambulatory arthroscopic knee surgery under standardized general anesthesia

• Surgery time does not exceed 80 minutes

• Patients without previous opioid and psychotropic medication

• Patients aged between 19 and 55 years, able to fill in the study questionnaire (Appendix F)

• Patients who have given written informed consent

Locations
Other Locations
Germany
University Medicine of Greifswald
RECRUITING
Greifswald
Contact Information
Primary
Taras Usichenko, MD, PhD
taras@uni-greifswald.de
00490383486
Backup
Joern Lange, MD, PhD
jnlange@uni-greifswald.de
00490383486
Time Frame
Start Date: 2019-02-01
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 60
Treatments
Experimental: Acupuncture
30 patients will receive acupuncture additionally to standard pharmacological therapy of postoperative pain
No_intervention: No intervention
30 patients will receive just standard pharmacological therapy of postoperative pain
Related Therapeutic Areas
Sponsors
Leads: University Medicine Greifswald

This content was sourced from clinicaltrials.gov