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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03415204
Other study ID # 0104-17-ZIV
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 20, 2017
Est. completion date December 20, 2018

Study information

Verified date January 2018
Source Ziv Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Post operative pain (POP) is a major obstacle on the road to healing, despite the increasing interest in postoperative pain management and development of pain control modalities (1). Postoperative pain is still insufficiently treated with more than 50% of patients suffering from moderate to severe pain early after surgery .Pain after orthopedic surgery is considered especially difficult to manage. Approximately half of total knee or hip arthroplasty patients present with extreme pain immediately after surgery. Total knee and hip arthroplasty often results not only in severe perioperative pain and debilitation, but chronic pain, joint stiffness, and functional disability many months or even years following the procedure. Various modalities of treating orthopedic POP exist, but the optimal management of postoperative pain remains controversial with no clear consensus of the best method.We suggest that acupuncture can be an effective treatment for post operative pain after total knee or hip arthroplasty.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date December 20, 2018
Est. primary completion date December 20, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - signed informed consent, above 18 years of age, about to undergo total knee or hip arthroplasty Exclusion Criteria: - Known mental disease, active cancer disease, coagulopathy, Hepatitis B,C.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
acupuncture
acupuncture for post operative pain

Locations

Country Name City State
Israel Ziv Medical Center Safed

Sponsors (1)

Lead Sponsor Collaborator
Ziv Hospital

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary average post operative pain during time of hospitalization post operative pain will measured twice daily - morning and afternoon during hospitalization time. patients will be asked to rate thier pain on a visual analog scale ranging from 0- no pain to 10 - severe pain average pain score during 5 days following operation
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