- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05201261
the Relationship Between Vertebral Body Length, Subarachnoid Space Width and Block Level
January 20, 2022 updated by: Yanchao Yang, Shengjing Hospital
Spinal anesthesia technology has been widely used in various surgeries and multi-mode analgesia.
Spinal ultrasound imaging has been proved to be a reliable tool for evaluating spinal parameters.
Ultrasound-guided spinal puncture technology has also been skillfully applied in clinical practice.
How to provide perfect nerve block effect for operation, provide good postoperative analgesia, and prevent unnecessary extensive block leading to other complications and related risks has always been the focus of anesthesiologists.
Doses and the relationship between the anesthesia plane great individual differences, and previous research on the patient's own condition such as height, weight, 6 to the anesthesia plane have different results, the influence of clinical work often refer patients height adjustment of drug doses, this research attempts to evaluate ultrasound was used to assess spinal vertebral body in the plane of the length and width of subarachnoid and anesthesia.
Study Overview
Status
Not yet recruiting
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
50
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
18 years to 55 years (ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients undergoing elective surgery under spinal anesthesia.
Inclusion criteria: (1) Elective lower extremity surgery; (3) ASA (American Society of Anesthesiologists) Grading: ⅰ - ⅲ.
Description
Inclusion Criteria:
- Patients undergoing elective lower limbs surgery
- ASA: grade I to III
Exclusion Criteria:
- There are contraindications to spinal anesthesia
- Allergic to local anesthetics
- Patient refused
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Ultrasound-guided group
Adult patients with American Society of Anesthesiologists physical status I/II/III scheduled to undergo elective Lower limb surgery under spinal anesthesia were considered for eligibility.
|
In the right decubitus position, the spine was scanned with an ultrasonic convex array probe.
Starting from the sacrum, the length of each vertebral body of the lumbar spine was measured on a para-midsagittal oblique view.
The intervertebral space was located and the width of the subarachnoid space was measured on a midsagittal and transverse view.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The length of lumbar cone
Time Frame: 1year
|
Ultrasound findings
|
1year
|
|
The width of subarachnoid space was measured by ultrasound
Time Frame: 1year
|
Ultrasound findings
|
1year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (ANTICIPATED)
February 1, 2022
Primary Completion (ANTICIPATED)
February 1, 2023
Study Completion (ANTICIPATED)
February 1, 2023
Study Registration Dates
First Submitted
December 16, 2021
First Submitted That Met QC Criteria
January 20, 2022
First Posted (ACTUAL)
January 21, 2022
Study Record Updates
Last Update Posted (ACTUAL)
January 21, 2022
Last Update Submitted That Met QC Criteria
January 20, 2022
Last Verified
December 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- block level
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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