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Suprainguinal Facia Iliaca Block in Maximizing the Feasibility of Positioning for Spinal Anesthesia

Effectiveness of Suprainguinal Facia Iliaca Block in Maximizing the Feasibility of Positioning for Spinal Anesthesia in Patients With Hip and Proximal Femur Fractures, a Placebo Randomized Controlled Study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07594366
Enrollment
40
Registered
2026-05-18
Start date
2022-09-01
Completion date
2026-01-30
Last updated
2026-05-18

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

Conditions

Spinal Anaesthetic Poisoning, Spinal Anaesthesia

Keywords

spinal anaesthesia positioning

Brief summary

In this study, we assessed the effect of suprainguinal facia iliaca block in maximizing the feasibility of positioning for spinal anaesthesia in patients with hip and proximal femur fractures by determining the angle that could be achieved and success rate of spinal anesthesia The control group received a sham block with the same technique of suprainguinal fascia iliaca block before being given spinal anaesthesia. The interventional group received suprainguinal fascia iliaca block before being given spinal anaesthesia.

Interventions

Fascia iliaca compartment block (FICB) was performed at the pre-anaesthesia holding area 30 minutes before shifting the patients to the operation room with 30 ml of 0.5% bupivacaine.

DRUGNormal Saline

Sham block was performed at the pre-anaesthesia holding area 30 minutes before shifting the patients to the operation room with 30 ml normal saline.

Sponsors

Suez Canal University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Masking description

The patient and the caregiver were blinded to the injectate in the procedure. The investigator was blinded to the solution that was used for the block, as a third person had prepared the injectate. The one who assessed the sitting angle was blinded to the group of the patient.

Intervention model description

* Group 1 - Fascia iliaca block with bupivacaine 0.5% was performed at the pre-anaesthesia holding area 30 minutes before shifting the patients to the operation room. * Group 2 - Sham block was performed at the pre-anaesthesia holding area 30 minutes before shifting the patients to the operation room with 30 ml normal saline. Each group included 20 patients. Fascia iliaca block was performed while patients were in the supine position with all aseptic precautions.

Eligibility

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

Inclusion criteria

* Patients are ASA I (American Society of Anesthesiologists physical status grade I) = normal healthy patients, ASA II (American Society of Anesthesiologists physical status grade II) = patients with mild systemic disease and no functional limitations, or ASA III (American Society of Anesthesiologists physical status grade III) = patients with moderate systemic disease and some functional limitations. * Patients having hip and/or proximal femur fractures.

Exclusion criteria

* Patient refusal to participate in the study * Patients' refusal for regional anaesthesia * Patients have other combined fractures rather than unilateral hip or proximal femur fractures. * Underlying coagulopathies. * Local infection. * Known allergy to LA. * Body mass index (BMI) more than 40 kg/m². * Heart block greater than first-degree. * Renal and hepatic dysfunction. * Neurological diseases such as Alzheimer's and dementia or apparent psychological instability.

Design outcomes

Primary

MeasureTime frameDescription
Degree of Fowler's position30 minutes after the fascia iliaca compartment block or sham block and till the full sitting position before spinal anaesthesia.Measure and compare the maximum tolerable degree of Fowler's position after fascia iliaca compartment block (FICB) and sham block in order to give spinal anaesthesia.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 19, 2026