Analgesia, Arthroplasty, Replacement, Knee
Conditions
Brief summary
Local anesthesia was performed on patients with total knee arthroplasty (TKA) through two different injection sites of local anesthetics and two local anesthetic drug . The pain score of patients after TKA was collected, then the analgesic effect of patients after TKA through two different injection sites and two different local anesthetic drug were analyzed and evaluated.
Interventions
PROCEDURENew local anesthesia injection site and new local anesthetic drug formulation.
The traditional injection site is the posterior joint capsule and the popliteal artery space (iPACK) plus multiple layers of tissues around the knee joint (posterior joint capsule, ligaments and subcutaneous tissue). The traditional local anesthetic formulation is 1% ropivacaine 10ml+ normal saline 40ml+10mg Morphine + 5mg dexamethasone. The new local anesthesia injection site is iPACK+Knee Cutaneous Nerve Block. The new local anesthetic formula is 1% ropivacaine 10ml+ normal saline 40ml+10mg morphine+1ml triamcinolone acetonide.
Sponsors
Diwuweilong
Study design
Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* 1\. Patients between the ages of 40-75, who meet the indications for total knee arthroplasty(TKA) surgery, plan to undergo unilateral TKA surgery, can tolerate surgical trauma, and have no surgical contraindications; * 2\. Patients who have good medical obedience and can cooperate to complete the evaluation of various indicators after the operation and continue to receive follow-up; * 3\. There is no contraindications to combined spinal-epidural anesthesia; * 4\. Agree to accept this trial and sign an informed consent form.
Exclusion criteria
* 1\. Allergic to test drugs; * 2\. Abnormal liver, kidney or heart function; * 3\. People who have chronic pain symptoms in other parts of the body other than the knee joint; * 4\. Patients with a history of multiple operations on the knee joint, or patients with abnormal anatomical structures; * 5\. Patients who cannot perform early functional exercise after unconventional knee replacement or other systemic diseases; * 6\. Cannot communicate with researchers normally.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change of the pain score before and after surgery | pre-operation, 6hours after surgery, 24hours after surgery, 48 hours after surgery. | A Visual Analogue Scale (VAS) is used to measure the amount of pain that a patient feels ranges across a continuum from none to an extreme amount of pain. Using a ruler, the score is determined by measuring the distance (mm) on the 10cm line between the no pain anchor and the patient's mark, providing a range of scores from 0-100. A higher score indicates greater pain intensity. |
Countries
China
Contacts
Primary ContactWeilong Diwu, M.M.
Outcome results
None listed