Adductor Canal Localization in Living and Cadaver
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorAnkara Etlik City Hospital
About this trial
The aim of this study is to define the starting and ending points of the adductor canal in adductor canal block (ACB) applications through distance measurements relative to the anterior superior iliac spine (ASIS) and the adductor tubercle. These measurements are performed using ultrasound (USG) and correlated with cadaveric data.
Key research questions addressed include:
* Can the start and end points of the adductor canal be formulated along a line drawn between the ASIS and the adductor tubercle? * Is there a definable relationship between the block application site and anatomical landmarks such as the vastoadductor membrane (VAM), the apex of the femoral triangle, and other adjacent structures that facilitates localization?
By validating ultrasound measurements with cadaveric findings, the study aims to provide researchers with a more predictable and reliable method for determining the optimal site for adductor canal block administration.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
None
Disqualifiers
None
Trial population
He study at Etlik City Hospital will include patients who meet the following criteria: ASA classification of 1, 2, or 3, indicating individuals who are healthy or have mild to moderate systemic disease without major functional limitation; a BMI below 35 to exclude participants with obesity-related comorbidities; and an age range of 18 to 65 to ensure a broad yet controlled sample while avoiding age-related confounding factors. All participants must also provide informed consent, confirming their understanding of the study's purpose, procedures, and potential risks.
Trial design
Design model
Case-control
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
200 Participants
are grouped into 2 trial groupsGroup A: ULTRASONOGRAPHIC PARTICIPANT GROUP
Group B: Cadaver Group
Trial outcomes
Primary outcomes
1
location of the adductor canal
Determine the location of the adductor canal on an imaginary line drawn between the anterior superior iliac spine and the adductor tubercle..
Time frame
Perioperative/PeriproceduralSecondary outcomes
1
Determining the entry point for adductor canal block
Standardization of the entry point for adductor canal block by defining the relationship of the canal to other structures
Time frame
Perioperative/Periprocedural2
Adductor Canal neighborhoods
Detection of the canal by imaging the Vasto adductor membrane
Time frame
Perioperative/Periprocedural3
cadaver dissection
Determining the compatibility of the data obtained in ultrasonographic imaging with the real anatomical structures after cadaver dissection
Time frame
Perioperative/Periprocedural4
adductor canal
measuring adductor canal length
Time frame
Perioperative/PeriproceduralSponsors and contacts
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Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: