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Ultrasound-Guided Oblique Short-Axis Adductor Canal Block.

Ultrasound-Guided Oblique Short-Axis Adductor Canal Block: Can the Oblique Approach Facilitate Perineural Catheter Insertion: A Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05587166
Enrollment
50
Registered
2022-10-19
Start date
2022-11-15
Completion date
2023-04-15
Last updated
2022-10-19

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

Conditions

Adductor Canal Block

Brief summary

The ideal pain management for knee surgery should provide excellent analgesia while minimizing opioid consumption and allowing early mobilization and rehabilitation. The use of the continuous technique in ACB allows the delivery of a larger quantity of local anaesthetic into the adductor canal than in the single-shot technique. The usual approach for ultrasound-guided ACB catheter insertion is through short-axis in-plane approach in which the ultrasound transducer is applied horizontally over the femoral artery and saphenous nerve. In this approach, the catheter is inserted through a 90-degree angulation with the nerve which might make the catheter insertion difficult. In the new oblique position, the catheter will be inserted in a less than 90-degree angulation. This study speculates that decreasing the angle of catheter insertion will make catheter insertion easier and faster.

Interventions

ultrasound-guided adductor canal block using oblique short-axis for catheter insertion

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* adult patients more than 18 years * ASA I-III * scheduled for unilateral knee surgery under spinal anesthesia with an adductor canal perineural catheter planned for postoperative pain control

Exclusion criteria

* Patient who had an allergy to any drug used in the study * Patients with neuropathy of any etiology in the affected extremity, hepatic or renal failure. * pregnant females * Patients who are unable to communicate with the investigators and hospital staff

Design outcomes

Primary

MeasureTime frame
catheter placement time (minutes)starting from time of syringe removal from placement needle to time of complete threading of the catheter at 20-cm mark measured in minutes and over 20 minutes

Contacts

Primary ContactAbeer Ahmed
abeer_ahmed@kasralainy.edu.eg01005244590

Outcome results

None listed

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