Evaluating the Midclavicle Block for Pain Management in Clavicle Fracture Surgery
Midclavicle Block: A Clinical Observational Study
This study is testing a new way to manage pain during surgery for broken collarbones to see if it helps patients feel better during and after the procedure.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 30 (estimated) |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Sponsor | Hospital HM Nou Delfos Academic / other |
| Locations | 1 site (Barcelona) |
| Trial ID | NCT06905249 on ClinicalTrials.gov |
What this trial studies
This observational study assesses the effectiveness and safety of the ultrasound-guided Midclavicle Block (MCB) as an anesthetic technique for patients undergoing surgery for midshaft clavicle fractures. The study focuses on intraoperative pain control measured by the Visual Analog Scale (VAS) and evaluates secondary outcomes such as postoperative pain, sedation levels, and potential complications. Local anesthetic is administered via three injections around the fracture site, and data will be collected during and after the procedure for up to 24 hours. The study aims to provide insights into the efficacy of this regional anesthesia technique.
Who should consider this trial
Good fit: Ideal candidates include adult patients with midshaft clavicle fractures scheduled for surgical intervention.
Not a fit: Patients with allergies to local anesthetics, coagulopathy, or pre-existing neuromuscular disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve pain management for patients undergoing clavicle fracture surgery.
How similar studies have performed: While there is limited data on the specific Midclavicle Block, similar ultrasound-guided regional anesthesia techniques have shown promise in improving postoperative pain management.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult patients with midshaft clavicle fractures scheduled for surgery. * ASA I-III. * Signed informed consent. Exclusion Criteria: * Allergy to local anesthetics. * Coagulopathy or active anticoagulant therapy. * Infection at the puncture site. * Pregnant or breastfeeding patients. * Pre-existing neuromuscular disorders.
Where this trial is running
Barcelona
- Hospital HM Nou Delfos — Barcelona, Spain (Recruiting)
Study contacts
- Study coordinator: Hipolito Labandeyra Gonzalez, MD, PhD, Anesthesiologist
- Email: hipolitolabandeyra@gmail.com
- Phone: +34696055181
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.