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Feasibility Study of Peripheral Venous Cannulation Pain in Predicting Acute Pain After Total Knee Arthroplasty

Not yet recruiting
Conditions
Venous Cannulation Pain
Movement-evoked Pain
Total Knee Arthroplasty
Acute Pain
Registration Number
NCT06002724
Lead Sponsor
RenJi Hospital
Brief Summary

The goal of this prospective observational study is to explore the feasibility of preoperative peripheral venous cannulation pain score in predicting acute pain after total knee arthroplasty, including resting pain and movement-evoked pain.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
180
Inclusion Criteria
  1. Patients undergoing the first unilateral total knee arthroplasty surgery under general anesthesia combined with nerve block ;
  2. Age : 18 years old ≤ age ≤ 80 years old ;
  3. ASA grade I-II ;
  4. Informed consent was signed by patients or immediate family members before operation.
Exclusion Criteria
  1. There are known pain abnormalities, mental disorders, cognitive dysfunction ;
  2. patients with long-term use of opioids and a history of drug dependence ;
  3. patients with alcohol dependence ;
  4. the patient refused to use the analgesic pump ;
  5. Difficult to understand the VAS score ;
  6. body mass index ≥ 40 ;
  7. hand nerve abnormalities, hand loss ;
  8. plan postoperative ICU patients ;
  9. In other cases, the researchers believe that is not suitable for this researcher.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
postoperative resting pain and movement-evoked painone hour、the first day and the second day after operation

visual analogue scale(VAS) of one hour、the first day and the second day after operation

Secondary Outcome Measures
NameTimeMethod
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