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Comparison Between Functional Outcomes of Flexor Tendon Repair Under WALANT and Brachial Plexus Block

Comparison Between Functional Outcomes of Flexor Tendon Repair Under Wide Awake Local Anesthesia no Tourniquet and Brachial Plexus Block

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06149962
Enrollment
30
Registered
2023-11-29
Start date
2023-07-10
Completion date
2024-07-10
Last updated
2023-11-29

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

Conditions

Flexor Tendon Rupture

Brief summary

Although outcomes after flexor tendon repair have reportedly improved with modern treatment, complications are common. Early passive and active motion protocols have improved outcomes of flexor tendon repairs. One potential complication of early motion occurs when the forces produced by this motion exceed the strength of the repair, which leads to gap formation and inhibits healing. Wide Awake Local Anesthesia No Tournique (WALANT) is a new anesthesia technique that has gained popularity among plastic surgeons. It was developed by Dr. Lalonde in Canada, and it involves the use of Lidocaine and adrenaline in the surgical site to control bleeding without the need for a tourniquet. Peripheral nerve blocks are overall safe when performed correctly, there are rare but serious risks associated with them. Risks include block failure, bleeding, infection, damage to surrounding structures, permanent nerve injury, and intravascular uptake of local anesthetic resulting in systemic toxicity.

Detailed description

WALANT can be applied in both elective and emergency surgeries and is commonly used for procedures involving the hand, wrist, and fingers, such as root tunnels syndromes, trigger finger, and fractures. However, it has some limitations and contraindications, including patients with coagulopathy or on anticoagulant therapy, those with allergies to any of the anesthesia components, or patients with a history of psychiatric disorders or aggressive behavior. Infraclavicular brachial plexus block (ICBPB) is widely used for anesthesia or analgesia during surgery on the hand and forearm. Today, it is most frequently performed using a sagittal ultrasound scan at the lateral infraclavicular fossa (LICF), where the local anesthetic is injected deep to the pectoral muscles. Peripheral nerve blocks are overall safe when performed correctly, there are rare but serious risks associated with them. Risks include block failure, bleeding, infection, damage to surrounding structures, permanent nerve injury, and intravascular uptake of local anesthetic resulting in systemic toxicity.

Interventions

PROCEDUREFLEXOR TENDON REPAIR

we will repair tendon of FDP only using 6 strand technique using PDS 4/0 core suture - prolene 6/0 running suture under WALANT technique and brachial plexus block.

Sponsors

Sohag University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
16 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Cooperative patients . * age between 16-60 years. * Acute flexor tendon injuries of the hand in both genders in medial four fingers. * Sharp mechanism of injury. * Single level injury zone 2.

Exclusion criteria

* Associated fractures close to the tendon injury. * Vascular injury requiring revascularization * Multiple level injury * Combined flexor and extensor laceration * Insufficient skin and soft tissue coverage * Tendon substance loss * Patients with coagulopathy or on anticoagulant therapy * Patients with allergies to any of the anesthesia components

Design outcomes

Primary

MeasureTime frameDescription
Quick Disabilities of the Arm, Shoulder, and Hand6 monthsQuick Disabilities of the Arm, Shoulder, and Hand using (DASH) scores

Countries

Egypt

Contacts

Primary ContactOMAR M HUSSEIN, resident
OMARMOHAMED@MED.SOHAG.EDU.EG01097195683
Backup ContactTAREK A ABULEZZ, professor

Outcome results

None listed

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