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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04757805
Other study ID # STUDY00000558
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 6, 2021
Est. completion date March 21, 2022

Study information

Verified date January 2023
Source Nationwide Children's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Although the current standard for lumbar puncture and spinal anesthesia is the use of manual palpation of surface landmarks to identify the correct interspace, performance of the procedure at too high of a level may increase the incidence of adverse effects. The current study will evaluate the efficacy of ultrasound in identifying the correct intervertebral space for lumbar puncture thereby improving the safety of the procedure.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date March 21, 2022
Est. primary completion date March 21, 2022
Accepts healthy volunteers No
Gender All
Age group N/A to 12 Months
Eligibility Inclusion Criteria: - Patients less than 1 year of age scheduled for spinal anesthesia for elective lower abdominal, urologic, or lower extremity surgery at Nationwide Children's Hospital Exclusion Criteria: - Parents unwilling for their children to undergo spinal anesthesia for surgery. - Children with known spinal anomalies including sacral dimple. - Children with coagulation abnormalities or receiving anticoagulation which precludes the use of spinal anesthesia. - Children with superficial or deep infections over the spine which precludes the use of spinal anesthesia.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Ultrasound
Ultrasound to locate the appropriate lumbar interspace to perform spinal anesthesia.

Locations

Country Name City State
United States Nationwide Children's Hospital Columbus Ohio

Sponsors (1)

Lead Sponsor Collaborator
Nationwide Children's Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Intended Interspace The vertebral interspace that the anesthesia provider believes that they had marked & identified by manual palpation Immediately prior to spinal anesthesia
Primary Actual Interspace of Provider's Mark The actual vertebral interspace that the anesthesia provider marked & identified, as verified by ultrasound. Immediately prior to spinal anesthesia
Secondary Level of Conus Medullaris - Sitting Assessing the level of the conus medullaris by ultrasound in the sitting position. Immediately prior to spinal anesthesia
Secondary Time to Mark The amount of time if took for the anesthesia provider to manually palpate and mark the desired interspace. Immediately prior to spinal anesthesia
Secondary Time to Conduct Ultrasound The amount of time it took for the investigator to identify the actual space that the provider marked using ultrasound. Immediately prior to spinal anesthesia
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