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

Feasibility Study of Peripheral Venous Cannulation Pain in Predicting Acute Pain After

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06002724
Enrollment
180
Registered
2023-08-21
Start date
2023-08-30
Completion date
2024-08-30
Last updated
2023-09-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Pain, Movement-evoked Pain, Total Knee Arthroplasty, Venous Cannulation Pain

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.

Interventions

None listed

Sponsors

RenJi Hospital
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
postoperative resting pain and movement-evoked painone hour、the first day and the second day after operationvisual analogue scale(VAS) of one hour、the first day and the second day after operation

Contacts

Primary ContactLiqin Tao
1349468702@qq.com18020264650

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026