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US Guided WALLANT vs CPB Block for Clavicle Surgery

Ultrasound Guided Wide Awake Local Anesthesia Versus Clavipectoral Fascia Plane Block With Superficial Cervical Plexus Block for Clavicle Surgery, Prospective Randomized Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06106399
Acronym
WALANT-CPB
Enrollment
42
Registered
2023-10-30
Start date
2023-08-01
Completion date
2024-03-01
Last updated
2023-10-30

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

Conditions

Clavicle Fracture, Clavicle Injury

Keywords

wide awake local anesthesia, clavipectoral fascia plane block, clavicle surgery

Brief summary

The clavicle is frequently fractured bone. regional anesthesia (RA) for clavicle surgery is always challenging due t complex innervation from the two plexuses (cervical and brachial). various RA techniques described for clavicle surgery include plexus blocks, fascial plane blocks,and truncal blocks.

Detailed description

Clavipectoral Fascial Plane Block (CPB) is most commonly used as an anesthesia and postoperative analgesia technique to clavicle surgery. This study is deigned to evaluate the feasibility of wide awake local anesthesia no tourniquet (WALANT) technique as a sole anesthesia in clavicle surgery, clavipectoral (CVP) fascia plane block + superficial cervical plexus plane block (CPB) as a sole anesthesia technique in clavicle surgery by using intraoperative verbal rating score (VRS) to determine how many patients need analgesia, sedation or convert to general anesthesia (GA), and postoperative assessment of patient satisfaction and 24 hour postoperative opioid consumption.

Interventions

PROCEDUREWALLANT

Comparison between (WALLANT) and (CPB) as a sole anesthesia in clavicle surgery

Sponsors

Al-Azhar University
Lead SponsorOTHER

Study design

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

Masking description

The patient and the anesthiologist who perform postoperative pain will not know the group.

Intervention model description

2 Arms model

Eligibility

Sex/Gender
ALL
Age
21 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* American society of anesthesiologists (ASA) 1,2 * Unilateral clavicle fracture.

Exclusion criteria

* psychologically unstable patient. * uncooperative patient. * patient refusal to be awake during surgery. * allergy. * infection at site of infection.

Design outcomes

Primary

MeasureTime frameDescription
efficacy of the block as a sole anesthetic technique6 monthsintra-operative verbal rating score to determine how many patients need supplementary analgesia,sedation or converted to general anesthesia

Secondary

MeasureTime frameDescription
24 hour postoperative opioid consumption6 monthsPost-operative hourly VAS for the first 6 hours, at 8 hours, at 12 hours, at 16 hours,then at 24 hours postoperative
patient satisfaction6 monthspatient satisfaction score immediately postoperative on hospital discharge and after 24 hours

Countries

Egypt

Contacts

Primary ContactIsmail M Ahmed, Prof
ismailabdelgawad.623@azhar.edu.eg00201117310053

Outcome results

None listed

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