Comparison of Lateral Decubitus and Upright Sitting Positions in Measuring Intervertebral Space Via Ultrasound in Obese Volunteers

December 23, 2025 updated by: Emre Sanci, Kocaeli City Hospital
The aim of the study is to compare the lateral decubitus and upright sitting positions in determining the intervertebral space measured by ultrasound in participants whose body mass index was greater than 30 and older than eighteen years old. Additionally, comparison of the sagittal and long-axis paramedian oblique planes in determining the intervertebral space measured by ultrasound in this group of volunteers. Furthermore, assesment of the reliability of measurements performed by practitioners with varying levels of ultrasound experience.

Study Overview

Status

Enrolling by invitation

Detailed Description

The study will be conducted in the Emergency Medicine Clinic of University of Health Sciences Kocaeli City Hospital. Participants over the age of 18 with a body mass index (BMI) of 30 or higher presenting to the emergency department will be included. After providing verbal information about the study, written informed consent will be obtained from participants who agree to take part. Participants will be evaluated by attending physicians in the emergency department, who will then inform the study investigators.

The upright sitting position is defined as the patient sitting upright on the stretcher with their legs hanging down the side, feet not touching the ground, and arms extended forward for support. The lateral decubitus position is defined as the patient lying on their side with their shoulders and hips perpendicular to the stretcher, knees flexed, and pulled toward the chest.

The ultrasound applications will be performed by two study investigators: one emergency medicine specialist with advanced ultrasound training and one with basic ultrasound training. Measurements will be taken first in the participant's preferred position (upright sitting or lateral decubitus) and then in the alternate position.

Since the traditional method for identifying the lumbar puncture (LP) site-known as Tuffier's line (the midpoint of the line connecting both anterior superior iliac spines in the lumbar region)-can be misleading in obese patients, the application site will be determined via ultrasound. An Esaote MyLab™ Gamma ultrasound device will be used, with the Esaote SL1543 linear probe as the first choice. If the linear probe does not provide adequate depth due to obesity, the Esaote SP2730 curved probe will be used.

For ultrasound application, the probe will initially be placed transversely just above the intragluteal fold, with the indicator pointing to the patient's left shoulder. Once the midline is identified, measurements will be performed in two planes: sagittal and long-axis paramedian oblique.

For the sagittal plane, the probe will be rotated 90 degrees with the indicator pointing toward the patient's head.

For the long-axis paramedian oblique plane, the probe will also be rotated 90 degrees toward the head but moved 1-2 cm laterally from the midline and angled slightly medially.

The probe will then be moved superiorly until the L4-L5 interspinal space is identified. The intervertebral space is defined as the hypoechoic region between hyperechoic spinous processes. Measurements will be taken from the L4-L5 and L3-L4 intervertebral spaces.

Each practitioner's measurements will include the distance to the ligamentum flavum, as well as data on whether the patient has undergone lumbar surgery, and their weight and height. These will be recorded in a pre-prepared standard data form. Practitioners will be blinded to each other's measurements to maintain objectivity.

Study Type

Observational

Enrollment (Estimated)

54

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

Healthy volunteers who want to participate in the study will be included.

Description

Inclusion Criteria:

  • participants whose body mass index was greater than 30
  • participants older than eighteen years old.

Exclusion Criteria:

  • participants who have a history of lumbar surgery
  • participants who have an infection on the lombar region
  • pregnant volunteers

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Comparison of Lateral Decubitus and Upright Sitting Positions in Ultrasound Measurement of Intervertebral Space in Adults with a BMI Over 30
Time Frame: Baseline
The primary outcome of the study is to compare the lateral decubitus and upright sitting positions in determining the intervertebral space measured by ultrasound in participants whose body mass index was greater than 30
Baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Comparison of Sagittal and Paramedian Oblique Planes for Ultrasound Measurement of Intervertebral Space
Time Frame: Baseline
The secondary outcome measure was comparison of the sagittal and long-axis paramedian oblique planes in determining the intervertebral space measured by ultrasound in participants whose body mass index was greater than 30.
Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 1, 2025

Primary Completion (Estimated)

October 1, 2026

Study Completion (Estimated)

December 31, 2026

Study Registration Dates

First Submitted

March 2, 2025

First Submitted That Met QC Criteria

December 23, 2025

First Posted (Estimated)

January 2, 2026

Study Record Updates

Last Update Posted (Estimated)

January 2, 2026

Last Update Submitted That Met QC Criteria

December 23, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 2021-120

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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