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PECS II Versus ICBN Block Plus SCNB for AV Fistula Creation in CRF Patients

Comparison Between Ultrasound-guided Pectoral Nerves Block Type II and Intercostobrachial Nerve Block as a Supplement to Supraclavicular Block for Anesthesia of Proximal Arteriovenous Access in End-stage Renal Disease Patients

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04988776
Enrollment
40
Registered
2021-08-03
Start date
2020-02-01
Completion date
2021-02-28
Last updated
2021-09-20

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

Conditions

Intraoperative Analgesia, Postoperative Pain

Brief summary

Brachial plexus block (BPB) is often utilized for proximal arm arteriovenous access creation. However, the medial upper arm and axilla are often inadequately anesthetized, as the Intercostobrachial nerve (which provides sensory supply to the axilla, upper medial arm, and a small area at the upper lateral chest) is not a component of the brachial plexus. This requires repeated, an intraoperative local anesthetic (LA) supplementation up to conversion into GA. The intercostobrachial nerve (ICBN) is a purely sensory nerve that arises primarily from the second intercostal nerve (T2) with occasional contribution from T3. Therefore, It is not a component of the brachial plexus and is not anesthetized by brachial plexus blockade. The ICBN can be blocked together with other nerves, such as the pectoral, intercostal, and long thoracic nerves in a recently described technique named pectoral nerves block type II (PECS II ).In this thesis, investigators compared the use of the PECS II block and ICBN block as a supplement to supraclavicular brachial plexus block for providing complete anesthesia of the upper arm for fistula creation surgery.

Interventions

OTHERultrasUltrasound-guided Intercostobrachial nerve block supplemental to supraclavicular block with 30 ml 0.25% bupivacaine (15 ml 0.5% bupivacaine will be added to 15 m

patients recieved ultrasound-guided Intercostobrachial nerve block with 10 ml 0.25% bupivacaine (5 ml 0.5% bupivacaine will be added to 5ml 0.9% normal saline ) supplemental to supraclavicular block with 30 ml 0.25% bupivacaine (15 ml 0.5% bupivacaine will be added to 15 ml of 0.9 %Nacl ) .

OTHERultrasound-guided pectoral nerves block type II supplemental to supraclavicular block

Patients received ultrasound-guided pectoral nerves block type II with 10 ml 0.25% bupivacaine (5 ml 0.5% bupivacaine will be added to 5ml 0.9% normal saline ) supplemental to supraclavicular block with 30 ml 0.25% bupivacaine (15 ml 0.5% bupivacaine will be added to 15 ml of 0.9 %Nacl )

Sponsors

Mamdoh Elsayed Lotfy
CollaboratorUNKNOWN
amany aly sultan
CollaboratorUNKNOWN
reem gaber abdel-mageed
CollaboratorUNKNOWN
Menoufia University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* ESRD patients. * Proximal Arm Arteriovenous Access Surgery. * Elective or emergency surgery * American Society of Anesthesiology (ASA) physical status II to III.

Exclusion criteria

* Inability of the patient to provide informed consent, communicate or cooperate * History of allergy to local anesthetics. * Preexisting upper limb neurological disease at the side of the surgery. * Patients on anticoagulant therapy or with history of coagulopathy. * Previous surgery at or near the site of the study. * The presence of skin infection at the puncture site.

Design outcomes

Primary

MeasureTime frameDescription
intraoperative local anesthetic requirement1-2 hours after surgery startvolume of local anesthetic

Secondary

MeasureTime frameDescription
postoperative pain24 hours after end of surgeryVisual analogue score (0-10) where 0=no pain and 10=the worst pain

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026