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Effect of Different Approaches to Brachial Plexus Nerve Block on medium term Primary Patency of Autogenous Arteriovenous Fistulas

Effect of Different Approaches to Brachial Plexus Nerve Block on medium term Primary Patency of Autogenous Arteriovenous Fistulas

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089838
Enrollment
Unknown
Registered
2024-09-18
Start date
2023-10-24
Completion date
Unknown
Last updated
2024-09-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

End-stage renal end-stage

Interventions

Group Local Anesthesia:20 ml of 0.5% ropivacaine injection for local infiltration anesthesia at the surgical site of the patient
Group Interscalene Brachial Plexus Block:Ultrasound guided interscalene Brachial Plexus Block
Group Axillary Brachial Plexus Block:Ultrasound guided Axillary Brachial Plexus Block

Sponsors

The First Affiliated Hospital of Guangzhou University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) ASAII~III, age range: > 18 years old, gender is not limited; (2) Those who meet the diagnostic criteria for end-stage renal failure and require maintenance hemodialysis (3) Patients who have undergone standard arteriovenous fistuloplasty for the first time in our hospital; (4) Vascular conditions suitable for wrist autologous arteriovenous fistuloplasty; (5) Patients and their families are informed and have signed a written informed consent form, and are willing to cooperate with the follow-up.

Exclusion criteria

Exclusion criteria: (1) Refusal of the patient and his/her family to participate in the study; (2) Allergy to anesthetic drugs; (3) Infection at the surgical site or nerve block skin puncture site; (4) Combined with severe decompensated important organ diseases; (5) Patients with coagulation dysfunction; (6) Patients with brachial plexus injury; (7) Have a history of any illness that may affect protocol compliance (such as severe mental disorder, cognitive dysfunction, substance abuse or addiction, etc.); (8) Patients judged by the investigator to be unsuitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
primary patency at 3 months;Diameter and blood flow of the cephalic vein, radial artery, and brachial artery before and after anesthesia;

Secondary

MeasureTime frame
Oxygen saturation;Non-invasive blood pressure;Physician satisfaction;

Countries

China

Contacts

Public Contactzheng junyi

Department of Anesthesiology, The First Affiliated Hospital of Guangzhou University of Chinese Medicine

zhangchi9908@163.com+86 137 6337 7393

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026