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The Analgesic Efficacy of Ultrasound Guided Anterior Femoral Cutaneous Nerve Block (AFCNB) in Combination with Femoral Triangle Block (FTB) versus Adductor Canal Block (ACB) in Total Knee Arthroplasty (TKA).

The Analgesic Efficacy of Ultrasound Guided Anterior Femoral Cutaneous Nerve Block (AFCNB) in Combination with Femoral Triangle Block (FTB) versus Adductor Canal Block (ACB) in Total Knee Arthroplasty (TKA).

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202312753143536
Enrollment
60
Registered
2023-12-11
Start date
2022-12-30
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Anaesthesia

Interventions

Anterior Femoral Cutaneous Nerve Block in Combination with Femoral Triangle Block
Adductor Canal Block

Sponsors

faculty of medicine ain shams university
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: a- Physical Status: ASA (American society of Anesthesiologists) I to III. b- Both sexes. c- Aged from forty to eighty years old. d- Scheduled for elective primary total knee arthroplasty due to osteoarthritis under spinal anesthesia.

Exclusion criteria

Exclusion criteria: a) Patient`s refusal of the procedure or to participate in the study. b) Patients with major spine deformities preclude spinal anesthesia. c) Patients with bleeding disorders and/or coagulopathy. d) Infection at the injection sites. e) Known allergy to local anesthetics. f) Patients with pre-existing myopathy or neuropathy. g) Uncooperative patients with significant cognitive dysfunction or psychiatric illness. h) Patients receiving any type of intraoperative periarticular infiltration (PAI) of local anesthetic by the surgeons. i) Failed spinal anesthesia.

Design outcomes

Primary

MeasureTime frame
The primary outcome of the study is to compare the time of the postoperative first request of the rescue analgesic in case of certain pain severity assessed by VAS between the two groups.

Secondary

MeasureTime frame
the total rescue opioids consumption, onset of ambulation, safety and complications of the used nerve blocks for the first 24 hours postoperatively.

Countries

Egypt

Contacts

Public Contactmohame el razzaz

assistant lecturer of anesthesia and intensive care ain shams university

mohamed.h.saleh@med.asu.edu.eg002723497108

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026