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

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06281431
Enrollment
1000
Registered
2024-02-28
Start date
2023-06-12
Completion date
2025-09-30
Last updated
2024-08-14

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

Conditions

Chronic Postoperative Pain

Keywords

Visualized nerve block needle, Acute pain, Chronic pain

Brief 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.

Detailed description

Surgical pain is one of the common complications after surgery, which seriously affects the recovery and treatment quality of patients. More than 20% of patients will suffer from postoperative chronic pain. According to the data of the National Bureau of Statistics, there are more than 70 million surgeries in China every year. Nerve block is one of the most commonly used methods for postoperative pain management in clinical practice. In recent years, the developing nerve block needle has gradually begun to be used in clinical practice. Compared with the ordinary non-developing nerve block needle, it may have a better effect on pain management after surgery, but whether it has a reduction effect on chronic pain after surgery is still unknown. The purpose of this study is to explore the effect of developing nerve block needle on postoperative pain, and to compare the difference between it and the common non-developing nerve block needle, so as to provide new ideas and methods for postoperative pain management.

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.

Sponsors

The Second Affiliated Hospital of Chongqing Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

1. The age is above 18 years old and below 70 years old. 2. patients whose surgical sites were in the chest, abdomen, upper limbs or lower limbs, including lobectomy, cholecystectomy, gastrointestinal resection, hysterectomy and other elective operations. 3. This operation was the first operation during the hospitalization. 4. Consent to participate in this study and sign an informed consent form.

Exclusion criteria

1. Patients with a history of alcohol or drug addiction. 2. Patients with disturbance of consciousness before operation. 3. Other conditions considered by the attending physician or researcher to be inappropriate for the study; 4. History of chronic pain. 5. Abnormal coagulation function.

Design outcomes

Primary

MeasureTime frameDescription
Chronic postoperative painThe third month after surgery.Incidence of Chronic pain assessment from 3 months after surgery
Moderate to severe painfrom end of surgery to 24 hours after surgery.Pain intensity (assessed by number rating scale, 0 represents no pain, 10 represents intolerable pain) more than 4

Secondary

MeasureTime frameDescription
Acute postoperative painFrom the ending of surgery to leaving the postanesthesia care unit, an average of 30 minutesPain intensity (assessed by number rating scale, 0 represents no pain, 10 represents intolerable pain) more than 4
Puncture operation timeFrom the ending of surgery to leaving the postanesthesia care unit, an average of 30 minutesTime from needle insertion to needle extraction
Number of needle passesFrom the ending of surgery to leaving the postanesthesia care unit, an average of 30 minutesThe number of times the needle is withdrawn more than 2 cm and resited

Countries

China

Contacts

Primary ContactHe Huang, ph.D
huanghe@cqmu.edu.cn13708385559
Backup ContactDa gang Wang, ph.D
kuanrenlunli@qq.com023 63693014

Outcome results

None listed

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