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Stellate Ganglion Block for Preserving Arteriovenous Fistula in Hemodialysis Patients Undergoing Major Lower Limb Orthopedic Surgery

Stellate Ganglion Block for Preserving Arteriovenous Fistula in Hemodialysis Patients Undergoing Major Lower Limb Orthopedic Surgery: A Randomized Controlled Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06300658
Enrollment
50
Registered
2024-03-08
Start date
2024-03-09
Completion date
2025-02-28
Last updated
2025-02-28

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

Conditions

Arteriovenous Fistula, Hemodialysis, Major Lower Limb Orthopedic Surgery, Stellate Ganglion Block

Brief summary

The aim of this study is to evaluate the role of stellate ganglion blockade (SGB) for preserving arteriovenous fistula in hemodialysis patients undergoing major lower limb orthopedic surgery.

Detailed description

The best way for dialysis in chronic renal failure (CRF) patients with consideration of feasibility, rate of infection, and patency is hemodialysis by using native access by using arteriovenous fistula (AVF). Altered calcium and phosphor metabolism in CRF patients would also increase vascular reactivity. Stellate ganglion blockade (SGB) has been used for several years for both diagnosis and treatment of circulatory problems in upper extremity. Recently preemptive SGB has been used in prevention of radial artery spasm in coronary artery patients. SGB increases blood flow and decrease vascular resistance in the arm. SGB prevents or ameliorates the reactivity of the muscular layer of the RA in response to both surgical manipulation during harvesting the artery and to the potent vasoconstrictor mediators released during surgery

Interventions

DRUGStellate ganglion block

Patient will receive preemptive stellate ganglion block (SGB) just before spinal anesthesia.

Sponsors

Aswan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Age 21 to 75 years. * Both sexes. * American Society of Anesthesiologists (ASA) physical status III. * Chronic renal failure (CRF) patients. * Undergoing major lower limb orthopedic surgery.

Exclusion criteria

* Psychiatric disorders. * History of substance abuse. * Ipsilateral brachial and radial artery stenosis. * Allergy to local anesthetics. * Cardiovascular and respiratory disorders. * Coagulopathy. * Use of vasoactive medications. * Obesity (body mass index \>30 kg/m2). * Smoking.

Design outcomes

Primary

MeasureTime frameDescription
Fistula flow rate7th day postoperativelyFlow rate will be measured on the first day postoperative then on the 7th day.

Secondary

MeasureTime frameDescription
Peak systolic velocity (PSV)7th day postoperativelyPeak systolic velocity (PSV) will be measured from radial artery 2 cm. proximal to fistula site, on the first day postoperative then on the 7th day.
End diastolic velocity (EDV)7th day postoperativelyEnd diastolic velocity (EDV) will be measured from radial artery 2 cm. proximal to fistula site, on the first day postoperative then on the 7th day.
Incidence of failure7th day postoperativelyIncidence of failure will be measured on the first day postoperative then on the 7th day.
Adverse effects7th day postoperativelyPostoperative adverse reactions such as hematoma, infection, thrombosis, bleeding, and pitosis will be recorded in both groups.

Countries

Egypt

Contacts

Primary ContactAyman M Eldemrdash, MD
ayman.mohamady@aswu.edu.eg00201001296116

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026