Pain management using a retroclavicular block for vascular surgery
Efficacy of Retroclavicular Dexamethasone With Bupivacaine in Patients Undergoing Upper Limb Vascular Surgeries
NA · New Valley University · NCT06406712
This study is testing a new way to manage pain during upper limb vascular surgery to see if it helps patients feel better and recover faster, especially when combined with a medication called dexamethasone.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 80 (estimated) |
| Ages | 20 Years to 65 Years |
| Sex | All |
| Sponsor | New Valley University (other) |
| Locations | 1 site (Asyut) |
| Trial ID | NCT06406712 on ClinicalTrials.gov |
What this trial studies
This study investigates the effectiveness of the retroclavicular approach for brachial plexus anesthesia in patients undergoing upper limb vascular surgery. The approach is known for its simplicity and potential benefits in pain management, including reduced postoperative opioid use and faster recovery times. The study will also explore the use of peri neural dexamethasone as an adjuvant to enhance analgesia provided by local anesthetics. By comparing outcomes with and without dexamethasone, the study aims to determine the optimal pain management strategy for these surgical patients.
Who should consider this trial
Good fit: Ideal candidates are patients scheduled for upper limb vascular surgery who do not have contraindications to regional anesthesia.
Not a fit: Patients with contraindications to regional blocks, such as coagulopathy or infection at the injection site, will not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve postoperative pain management and recovery for patients undergoing upper limb vascular surgery.
How similar studies have performed: Previous studies have shown positive outcomes with similar regional anesthesia techniques, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients undergoing upper limb vascular surgey . Exclusion Criteria: * \- Contraindications to regional block (coagulopathy, infection at the needle insertion site, or diaphragmatic paralysis). * Altered conscious level. * Pregnancy. * Body mass index (BMI \> 35). * Patients who have difficulty understanding the study protocol. * Patients who have any known contraindication to study medications. * Patient refusal.
Where this trial is running
Asyut
- Faculty of Medicine — Asyut, Egypt (RECRUITING)
Study contacts
- Principal investigator: ahmed ismail, lecture — faculty of medicine , new valley university
- Study coordinator: ahmed ismail, lecture
- Email: ahmed_ismail87@med.nvu.edu.eg
- Phone: 01097845491
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.
Conditions: Pain Management