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OpenTrials
Completed

NCT Number: NCT02697747

Identification of L3-L4 Interspace in Parturients

The investigators hypothesize that teaching ultrasound sonoanatomy to identify the L3-L4 interspace will improve resident's long term skill to correctly identify the interspace as compared to palpation alone.

Completed

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Key information

Age range

12 year–65 year

Sex eligibility

Female

Study type

Observational

Primary location

Beth Israel Deaconess Medical Center

Boston, Massachusetts, 02215, United States

About this study

This will be an observational education based study to improve anesthesiology resident's ability to correctly identify the L3-L4 interspace. Residents who agree to participate in the study will be trained using ultrasound to identify the L3-L4 interspace during their rotation on the obstetric anesthesia service. Training will include using the ultrasound to correlate the surface palpation with the underlying structures. This will be supplemented with teaching videos and literature. The training will be performed for the first three weeks of the four week rotation.

After undergoing this training program, during the fourth week of the rotation, the residents will be asked to perform palpation identification of the L3-L4 interspace on parturients. Ultrasound will be used to assess the accuracy of the identified level. These assessments will repeated at six and 12 months to assess whether the skill has been retained.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • term gestation (at least 38 weeks gestation)

Exclusion criteria

  • Prior back surgery
  • Previously diagnosed skeletal deformities such as scoliosis
  • BMI greater than 40
  • Height less than 60 inches
  • Patient discomfort requiring immediate analgesia

Treatment and study plan

Education

Other

Educational intervention in the use of ultrasound to identify landmarks

Primary outcomes

  1. Accuracy measured as percentage of cases where the L3-4 vertebral interspace is identified correctly

    Time frame: 1 month

    Percentage of cases where the L3-4 vertebral interspace is identified correctly

Secondary outcomes

  1. Durability measured as percentage of cases where the L3-4 vertebral interspace is identified correctly

    Time frame: 6 months and 12 months

    percentage of cases where the L3-4 interspace is identified correctly at 6 months and again at 12 months

Sponsors and collaborators

Lead sponsor

Beth Israel Deaconess Medical Center

Other

Registry information

Important dates

Study start
2015
Primary completion
2020
Study completion
2021
First posted
Mar 3, 2016
Registry last updated
Oct 1, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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