Cervical ESPB to help pain after proximal humerus repair
Official title: Evaluation of Analgesic Efficacy of Cervical Erector Spinae Plane Block in Proximal Humeral Fracture Surgery, A Motor-Sparing Block
Run by Menoufia University · NCT07824466 · Data updated 2026-11-12
This study tests whether a cervical erector spinae plane block helps manage postoperative pain after surgery to fix a proximal humeral fracture in adults under general anesthesia.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 70 Years |
| Sex | All |
| Enrollment | 44 (estimated) |
| Sponsor | Menoufia University Academic / other |
| Locations | 1 site (Shibīn al Kawm, Menoufia) |
| Status | Recruiting |
| Started | August 1, 2026 |
| Main results expected | July 1, 2027 |
| Study ends | July 1, 2027 |
| Registry record updated | September 17, 2026 |
| Trial ID | NCT07824466 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18–70 with ASA I–II status undergoing unilateral proximal humerus ORIF who consent and have no exclusions such as coagulopathy or local infection.
✕Probably not a fit
Patients with contraindications to regional anesthesia, significant comorbidities, or atypical pain responses may not experience benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
Proximal humeral fractures are common in older adults and can cause significant postoperative pain that hinders recovery. This trial investigates the cervical erector spinae plane block as a regional anesthesia technique to provide pain relief after ORIF of the proximal humerus. The block is intended to offer a wide sensory coverage with a potentially favorable safety profile, aiming to reduce opioid needs and improve rehabilitation. Eligible participants are adults 18–70 years old with ASA I–II status undergoing unilateral PHF ORIF, excluding those with coagulopathy, infection at the injection site, or contraindications to local anesthetics or opioids. The study is conducted at Menoufia University with a lead sponsor and no listed collaborators.
Why it matters
Potential benefit: If successful, participants may experience better postoperative pain control and potentially reduced opioid requirements after shoulder surgery.
How similar studies have gone: Previous regional anesthesia approaches have shown pain benefits in similar shoulder procedures, but the cervical ESPB for proximal humerus repair remains relatively novel in this context.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age: 18-70 years old. * Adults scheduled for unilateral proximal humerus open reduction and internal fixation (ORIF). * American Society of Anesthesiologists (ASA) physical status I-II patients. Exclusion Criteria: * Patient refusal. * Coagulopathy \[International Normalized Ratio (INR) \>1.4, platelets \<100,000/mm³\]. * Local infection at the block site. * Allergy to local anesthetics or opioids. * History of drug addiction or chronic opioid use. * Significant neurological or psychiatric disorders. * Hemodynamically unstable patients.
Where it's running
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Menoufia University
Shibīn al Kawm, Menoufia, Egypt Recruiting
Study contacts
- Study coordinator: Ahmed E Elharty, MBBCH
- Email: Ahmed.Alsyed55@med.menofia.edu.eg
- Phone: 00201000262671
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.