RecruitingNot ApplicableNCT06281431

A Comparative Effect of Echogenic Needle for Nerve Block on Acute and Chronic Postoperative Pain


Sponsor

The Second Affiliated Hospital of Chongqing Medical University

Enrollment

1,000 participants

Start Date

Jun 12, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

Surgical pain is a common complication after surgery, affecting patient recovery and treatment quality. \>20% of patients suffer from chronic postoperative pain. China has \>70 million surgeries yearly. Nerve block manages postoperative pain, with developing nerve block needles now used in clinics. Developed needles may have better pain management effects than non-developed ones, but their effect on reducing chronic pain remains unclear. This study aims to explore the effect of developed nerve block needles on postoperative pain and compare them to non-developed needles, providing new ideas and methods for pain management.


Eligibility

Min Age: 18 YearsMax Age: 70 Years

Inclusion Criteria4

  • The age is above 18 years old and below 70 years old.
  • patients whose surgical sites were in the chest, abdomen, upper limbs or lower limbs, including lobectomy, cholecystectomy, gastrointestinal resection, hysterectomy and other elective operations.
  • This operation was the first operation during the hospitalization.
  • Consent to participate in this study and sign an informed consent form.

Exclusion Criteria5

  • Patients with a history of alcohol or drug addiction.
  • Patients with disturbance of consciousness before operation.
  • Other conditions considered by the attending physician or researcher to be inappropriate for the study;
  • History of chronic pain.
  • Abnormal coagulation function.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

PROCEDUREEchogenic nerve block needle

A 22G 8-cm echogenic nerve block needle (LEAPMED, CHINA) is selected for the procedure, administered under ultrasound guidance. Subsequently, a volume of 20 ml 0.375% ropivacaine is injected at the needle's tip for analgesic effect. The spread of the medication will be assessed through short- and long-axis imaging perspectives. Following this, evaluations are conducted to assess acute postoperative pain as well as chronic postoperative pain. Parameters such as the duration of nerve blockade, the incidence of punctures, and any associated complications are all meticulously appraised.

PROCEDURENon-echogenic nerve block needle

A 22G 8-cm thin wall low bottom nerve block needle (KDL, CHINA) is selected for the procedure, administered under ultrasound guidance. Subsequently, a volume of 20 ml 0.375% ropivacaine is injected at the needle's tip for analgesic effect. The distribution of the medication will be assessed using short- and long-axis imaging perspectives. Following this, evaluations are conducted to assess acute postoperative pain as well as chronic postoperative pain. Parameters such as the duration of nerve blockade, the number of punctures, and any associated complications are all meticulously appraised.


Locations(1)

He Huang

Chongqing, Chongqing Municipality, China

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06281431


Related Trials