- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04092478
'' Abdominal Crunch Positions With the Others in Terms of Interspinous Distance in Adult Patients ''
''Compare Abdominal Crunch Positions With Conventional Sitting and Lateral Decubitus Positions in Terms of Interspinous Distance in Adult Patients''
The most important factor for ease of operation and safety during spinal anesthesia is the determination of the spinal space. Increasing lumbar flexion facilitates access to the spinal space. Traditionally, patients undergo spinal anesthesia with lateral or sitting lumbar flexion.
In a study by Martha L Walker et al., The maximum extension of the knees, adduction of the hip, and a modified sitting position with the back flexion, ie, the abdominal crunch position, were found to be effective in increasing the flexion of the lumbar spine.
In our study, we aimed to measure the interspinal distance with the abdominal crunch position with the help of ultrasonography (USG) and to compare the interspinal distance with the measurements obtained in traditional positions (sitting position and lateral decubitus).
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Interspinal distance will be measured by ultrasonography by 3 different positions, respectively, for the patients who will undergo elective surgery and meet the study criteria and give voluntary consent.
This evaluation process is to record and compare the measurement results. Patients will not undergo any interventional procedures.
Patients who have difficulty in positioning due to hip, femur, knee and tibial fractures or arthrosis and who cannot be communicated will not be included in the study.
One hundred of patients over the age of 18 who will undergo elective surgery will be included in the study.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Meram
-
Konya, Meram, Turkey, 42090
- Yasin Tire
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients over the age of 18
- Undergo elective surgery
Exclusion Criteria:
- Patients with vertebral anomaly
- Patient with not communicated
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Traditional Sitting Position
We are going to use the Traditional Sitting Position on each patients.
|
The patient positions during the spinal anesthesia
|
Lateral Decubitis Position
We are going to use the Lateral Decubitis Position on each patients.
|
The patient positions during the spinal anesthesia
|
Abdominal Crunch Position
We are going to use the Abdominal Crunch Position on each patients.
|
The patient positions during the spinal anesthesia
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Inter spinal distance
Time Frame: Through study completion, an average of 6 months.
|
Increasing of the Inter spinal distance
|
Through study completion, an average of 6 months.
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Yasin Tire, MD, Konya Meram State Hospital
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- YTire
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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