NCT07814703 Intercostobrachial Nerve Block vs Erector Spinae Block for Medial Arm A-V Fistula Surgery
| NCT ID | NCT07814703 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Fayoum University Hospital |
| Condition | Surgical Anesthesia |
| Study Type | INTERVENTIONAL |
| Enrollment | 158 participants |
| Start Date | 2026-04-01 |
| Primary Completion | 2027-04-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 158 participants in total. It began in 2026-04-01 with a primary completion date of 2027-04-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Comparison Between Ultrasound-guided Intercostobrachial Nerve Block with Supraclavicular Block versus Ultrasound -guided Erector Spinae block with Supraclavicular Block for Medial Arm A-V Fistula Surgery
Eligibility Criteria
Inclusion Criteria: * ESRD patient undergoing creation AVF in the medial side of the arm. Exclusion Criteria: * 1\. Patient refusal 2. Drug allergies 3. Body Mass Index of 35 kg/m² or more 4. Coagulation abnormalities 5. Severe heart, kidney, and liver diseases, 6. Pregnancy 7. Vasculitis 8. Unstable hemodynamics 9. Upper extremity neuropathy 10. Mental illness 11. Seizures 12. Contralateral chest problems 13. Infection at site of injection
Contact & Investigator
mohamed ahmed Ismail, professor
STUDY CHAIR
Faculty of medicine,Fayoum University
Frequently Asked Questions
Who can join the NCT07814703 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Surgical Anesthesia. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07814703 currently recruiting?
Yes, NCT07814703 is actively recruiting participants. Contact the research team at Taghreedshaban60@gmail.com for enrollment information.
Where is the NCT07814703 trial being conducted?
This trial is being conducted at Al Fayyum, Egypt.
Who is sponsoring the NCT07814703 clinical trial?
NCT07814703 is sponsored by Fayoum University Hospital. The principal investigator is mohamed ahmed Ismail, professor at Faculty of medicine,Fayoum University. The trial plans to enroll 158 participants.