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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorThe Second Affiliated Hospital of Chongqing Medical University

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

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.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Echogenic nerve block needle

    Procedure/Surgery

    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.

  • Non-echogenic nerve block needle

    Procedure/Surgery

    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.

Treatment groups

1,000 Participants
are divided into 2 treatment groups
Group A: Echogenic nerve block needleExperimental treatment 1 intervention
Group B: Non-echogenic nerve block needleOther 1 intervention

Trial outcomes

Primary outcomes

1

Chronic postoperative pain

Incidence of Chronic pain assessment from 3 months after surgery

Time frame
The third month after surgery.
2

Moderate to severe pain

Pain intensity (assessed by number rating scale, 0 represents no pain, 10 represents intolerable pain) more than 4

Time frame
from end of surgery to 24 hours after surgery.

Secondary outcomes

1

Acute postoperative pain

Pain intensity (assessed by number rating scale, 0 represents no pain, 10 represents intolerable pain) more than 4

Time frame
From the ending of surgery to leaving the postanesthesia care unit, an average of 30 minutes
2

Acute postoperative pain

Pain intensity (assessed by number rating scale, 0 represents no pain, 10 represents intolerable pain) more than 4

Time frame
From return to the ward to 12 hours after return to the ward
3

Acute postoperative pain

Pain intensity (assessed by number rating scale, 0 represents no pain, 10 represents intolerable pain) more than 4

Time frame
From 12 hours after return to the ward to 24 hours after return to the ward
4

Puncture operation time

Time from needle insertion to needle extraction

Time frame
From the ending of surgery to leaving the postanesthesia care unit, an average of 30 minutes

Other outcomes

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