← Back to all trials
Recruiting
NCT07833930
Incidence and Clinical Features of Breakthrough Pain After Brachial Plexus Block in Diabetic Patients
Conditions: Postoperative Pain
Sex: All
Ages: 18 Years – 80 Years
Healthy volunteers: Yes
Enrollment: 216
Sponsor: Second Hospital of Shanxi Medical University
Location: Second Hospital of Shanxi Medical University Taiyuan
Summary
This observational study aims to determine the incidence and clinical characteristics of rebound-breakthrough pain after ultrasound-guided brachial plexus block in adult patients with type 2 diabetes mellitus. Adult patients undergoing elective upper-extremity surgery are divided into a type 2 diabetes group and a non-diabetic control group. Baseline clinical data and pain-related outcomes are collected after nerve block. This work may provide evidence for optimizing perioperative pain management for diabetic patients receiving brachial plexus block.
Eligibility Criteria
Inclusion Criteria:
* Aged 18 years or older
* Undergoing elective upper-extremity surgery
* Planned for ultrasound-guided brachial plexus block with 0.375% ropivacaine
* Able to cooperate with pain assessment and follow-up within 48 hours after block
* Written informed consent obtained
Exclusion Criteria:
* Allergy or contraindication to amide-type local anesthetics
* Pre-existing peripheral neuropathy of the affected upper limb
* Chronic regular use of opioids before surgery
* Coagulopathy or infection at the block puncture site
* Cognitive dysfunction unable to complete NRS pain evaluation
* Pregnancy or lactation
* Incomplete clinical data expected during follow-up
Source: ClinicalTrials.gov (NCT07833930). StuddyBuddy aggregates publicly available trial information.