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

Not Applicable
Recruiting
Conditions
Chronic Postoperative Pain
Interventions
Procedure: Non-echogenic nerve block needle
Procedure: Echogenic nerve block needle
Registration Number
NCT06281431
Lead Sponsor
The Second Affiliated Hospital of Chongqing Medical University
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.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
1000
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.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Non-echogenic nerve block needleNon-echogenic nerve block needleUsing a common nerve block needle.
Echogenic nerve block needleEchogenic nerve block needleUsing a echogenic nerve block needle.
Primary Outcome Measures
NameTimeMethod
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 Outcome Measures
NameTimeMethod
Acute postoperative painFrom 12 hours after return to the ward to 24 hours after return to the ward

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

Number of needle passesFrom the ending of surgery to leaving the postanesthesia care unit, an average of 30 minutes

The number of times the needle is withdrawn more than 2 cm and resited

Puncture operation timeFrom the ending of surgery to leaving the postanesthesia care unit, an average of 30 minutes

Time from needle insertion to needle extraction

Trial Locations

Locations (1)

He Huang

🇨🇳

Chongqing, Chongqing, China

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