MedTrace Logo

Midclavicle Block: A Clinical Observational Study

NCT06905249 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2025-07-04

No results posted yet for this study

Summary

This prospective observational study aims to evaluate the effectiveness and safety of the ultrasound-guided Midclavicle Block (MCB) as an anesthetic and analgesic technique for midshaft clavicle fracture surgery. The primary objective is to assess intraoperative pain control using the Visual Analog Scale (VAS). Secondary outcomes include postoperative pain, sedation levels (Ramsay scale), motor and sensory block of the ipsilateral upper limb, hemidiaphragmatic paralysis, and hemodynamic stability. The requirement for rescue analgesia and the incidence of systemic complications will also be recorded. Intraoperative Qnox and Qcon monitoring will be used to explore potential correlations with pain and sedation levels. Data will be collected intraoperatively and postoperatively for up to 24 hours.

Conditions

  • Postoperative Pain Management
  • Regional Anaesthesia
  • Ultrasound Guided
  • Clavicle Fracture

Sponsors & Collaborators

  • Hospital HM Nou Delfos

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-12-02
Primary Completion
2025-05-31
Completion
2025-05-31

Countries

  • Spain

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06905249 on ClinicalTrials.gov