Comparing two methods of nerve block for creating arteriovenous fistulas
Comparison of Efficacy of Ultrasound-Guided Supraclavicular and Axillary Block for Arterio-Venous Fistula Creation: An Observer-Blinded, Non-inferiority Randomized Controlled Trial
NA · Sultan Qaboos University · NCT05809258
This study is testing which of two nerve block methods works better for pain relief in adults getting arteriovenous fistulas.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 120 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Sultan Qaboos University (other) |
| Locations | 1 site (Muscat) |
| Trial ID | NCT05809258 on ClinicalTrials.gov |
What this trial studies
This study compares the effectiveness of supraclavicular and axillary brachial plexus nerve blocks in providing analgesia for adults undergoing arteriovenous (AV) fistula creation. Both techniques will be performed under ultrasound guidance using the same local anesthetic. A total of 120 patients will participate, with 60 receiving each type of nerve block. The study aims to evaluate the need for additional analgesia, the recovery rate, and the overall efficacy of these regional anesthesia techniques. An interim analysis will be conducted after 30 patients have been recruited for each technique.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 years old who are scheduled for AV fistula creation in the antecubital fossa.
Not a fit: Patients who are hemodynamically unstable, have local infections, or known allergies to local anesthetics may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management and recovery for patients undergoing AV fistula creation.
How similar studies have performed: While there have been studies on brachial plexus blocks, this specific comparison using ultrasound guidance for AV fistula creation is novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age \>18 years old * Patients undergoing AV fistula creation in the antecubital fossa Exclusion Criteria: * - Patient Refusal * Hemodynamically unstable patient * Local infection over the insertion site * Coagulopathy * Known allergy to Local Anaesthetic medications * Abnormal anatomy * Use of antiplatelet within 7 days of surgery
Where this trial is running
Muscat
- Sultan Qaboos University Hospital — Muscat, Oman (RECRUITING)
Study contacts
- Principal investigator: Jyoti Burad, MD, EDIC — Sultan Qaboos University Hospital
- Study coordinator: Jyoti Burad, MD, EDIC
- Email: jyotiburad@yahoo.com
- Phone: +96899578636
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: Arteriovenous Fistula, Brachial Plexus Block, Clinical Efficacy, Arteriovenous fistula, brachial plexus block, ultrasound guided, complications, block recovery