Recruiting

COMPASS

Sponsor:

Seattle Children's Hospital

Code:

NCT01285531

Conditions

Lumbar Puncture

Eligibility Criteria

Sex: All

Age: 0 - 18

Healthy Volunteers: Not accepted

Interventions

Compass Lumbar Puncture Enhanced

Study Details

Brief summary:

Objective: To evaluate pediatric emergency department provider lumbar puncture success with and without the Compass Lumbar Puncture Enhanced, a new pressure transducer, in order to determine: the proportion of lumbar punctures where a) any cerebrospinal fluid is obtained on the first attempt, b) any cerebrospinal fluid is obtained on any attempt, and c) sufficient cerebrospinal fluid is obtained for standard tests (culture, chemistries, cell count); the time to provider success in obtaining a) a drop of fluid from the needle, and b) opening pressure measurement; the proportion of successful lumbar punctures that contain blood; and provider satisfaction.

Background: Lumbar punctures are necessary to diagnose meningitis, neurological diseases and some cancers. They are common pediatric emergency department procedures that frequently require repeated attempts or are only partially successful, with sufficient blood to limit interpretation. Measuring cerebrospinal fluid pressure during lumbar punctures is recommended but rarely done, due to limitations of current technology. Liquid column manometry is cumbersome, time-consuming and frequently impractical. Existing pressure transduction probes that connect via tubing to external monitors are not designed or recommended for lumbar punctures. The pressure is displayed on a monitor that is difficult to view during the LP procedure and they equilibrate too slowly to keep pace of pressure changes during LPs. The Compass Lumbar Puncture Enhanced is a new, inexpensive, disposable, medical device, specifically designed for use during LPs, that has the potential to increase lumbar punctures success and decrease blood contamination. It attaches to the spinal needle and displays both a numeric pressure value and a pressure waveform, allowing physicians to more readily identify the cerebrospinal fluid space and measure cerebrospinal fluid pressure. The device is small, easy to use, and readily incorporated into standard practice.

The Compass Lumbar Puncture Enhanced uniquely provides immediate feedback about pressure that may allow physicians to more quickly and confidently identify the CSF space, and instantly determine cerebrospinal fluid pressure when the space is reached. The investigators believe the Compass Lumbar Puncture Enhanced will increase lumbar punctures success and decrease the proportion containing blood. It has the potential to become the standard of care and be used in every lumbar puncture procedure. This study is expected to demonstrate the clinical utility of the Compass Lumbar Puncture Enhanced to the medical community. Increased awareness of the Compass Lumbar Puncture Enhanced and a positive demonstration of the viability of the technology will help attract either the investment capital or the strategic partnership necessary to fully develop the market.

Conditions

Lumbar Puncture

Study ID

NCT01285531

Start date

Jan, 2011

Status verified date

Feb, 2011

Primary completion date

Jan, 2012

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 0 - 18

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Age 0 - 18 years old
  • Patient was in the Seattle Children's Hospital (SCH) Emergency Department (ED)within 24 hours
  • Patient requires lumbar puncture (can be performed in the ED or inpatient, within 24 hours of arrival to the ED)
  • Parent is able to read English or Spanish
  • A provider who is trained in the use of the Compass device is willing and able to use it during the LP

Exclusion Criteria:

  • Child is a foster child or ward of the state or is unaccompanied by their legal guardian
  • Child has a lower spine deformity, such as spina bifida, that would impact lP success
  • The child is pregnant, by verbal report or clinically available test results

Study Design

Enrollment

60 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Diagnostic

Interventions and Outcome Measures

Arms

no intervention: Lumbar puncture

The participants randomly assigned to this arm will receive a lumbar puncture using standard procedures and equipment

experimental: Lumbar puncture with the Compass device

The participants randomly assigned to this group will receive a lumbar puncture with the use of the Compass device.

Interventions

Compass Lumbar Puncture Enhanced

Participants randomly assigned to this group will receive a lumbar puncture using the Compass device.

Primary outcome measure

  • Lumbar puncture success [ Time Frame: 1 minute to 2 hours ]

Central Contacts and Locations

Locations

Seattle Children's Hospital

Recruiting

Seattle, Washington, United States, 98105

Contacts

Principal Investigator:

Julie C Brown, MD, MPH

More Information

Sponsor

Seattle Children's Hospital

Last update posted

Feb 17, 2011

Last verified

Feb, 2011

Keywords

  • lumbar puncture
  • Compass
  • pressure transducer
  • manometry
  • The focus of the study is to improve lumbar puncture(LP)success, reduce the number of LP attempts, reduce the number of traumatic attempts.

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Seattle Children's Hospital on 2011-02-17.