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Evaluation of Lumbar Plexus Block Success With Near Infrared Spectroscopy (NIRS)

Near Infrared Spectroscopy (NIRS) Evaluation of Lumbar Plexus Block Success for Lower Extremity Orthopedic Surgery

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06126133
Enrollment
40
Registered
2023-11-13
Start date
2023-11-11
Completion date
2024-01-13
Last updated
2023-11-14

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

Conditions

Lumbar Plexus, Near Infrared Spectroscopy, Nerve Block

Brief summary

Tests such as the pin-prick test, cold application or the Bromage scale are currently used to measure the success of nerve blocks and are considered subjective assessments as they require verbal consent from the patient. Near Infrared Spectroscopy (NIRS) measures the differential absorption and reflection of near infrared light transmitted by human tissues, providing a tissue-oxygen saturation index. Modern NIRS-based instruments use multiple detectors to filter spectroscopy data from skin structures to detect subcutaneous tissue oxygenation. Successful regional anesthesia results in decreased sympathetic activity within the distribution of blocked nerves. Regional oxygen saturation (rSO2) has been shown to increase in innervated areas after sympathetic block.

Detailed description

The aim of this study was to show whether the success of lumbar plexus block applied in lower extremity orthopedic surgeries can be evaluated by Near Infrared Spectroscopy (NIRS), which is used to measure tissue oxygenation.

Interventions

DEVICENear Infrared Spectroscopy

Two NIRS probes will be attached to the extremity to be operated on and to the other lower extremity on the opposite side, at a level approximately coinciding with the midline above the quandriceps femoris muscle.

Sponsors

Bursa Yuksek Ihtisas Training and Research Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* 18-90 years old * femoral neck fracture, * femoral shaft fracture, * hip replacement surgery * who will undergo velumbar plexus block will be included in the study.

Exclusion criteria

* BMI\>40 kg/m2 * infection in the block area * peripheral neuropathy, * hemoglobinopathy * peripheral vascular disease * allergy to local anesthetics * patients with contraindications for lumbar plexus block

Design outcomes

Primary

MeasureTime frameDescription
rso240 minutesThe regional oxymetry probe will be placed in the the quandriceps femoris muscle, one on the extremity to be operated on and the other on the opposite lower extremity.

Secondary

MeasureTime frameDescription
sensory block level40 minutesThe sensory block level will be realised by cold testing at 10 minute intervals after applying the block.
blood pressure values40 minutessystolic, diastolic and mean blood pressure values will be recorded non-invasively in mmhg.
so240 minutesfingertip SO2 measured by pulse oximetry

Contacts

Primary ContactKorgün Ökmen, Assoc. PhD.
korgunokmen@gmail.com+905057081021

Outcome results

None listed

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