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NCT01643291 · ClinicalTrials.gov registry record · NA

Ultrasound Use for Difficult Lumbar Punctures in Pediatric Oncology Patients

A NA study, sponsored by Nationwide Children's Hospital.

Terminated
Registry status
NA
Development phase
3
Enrollment target

NCT01643291: Clinical Trial NA study, sponsored by Nationwide Children's Hospital.

NCT01643291 is a NA study that was terminated before completion, run by Nationwide Children's Hospital. The registered enrollment target is 3 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01643291, a NA study, was terminated before completion, sponsored by Nationwide Children's Hospital.

TERMINATED
Registry status
NA
Development phase
3 participants
Enrollment target

Study Summary

Hematology-oncology patients may require frequent lumbar puncture for diagnosis, assessment and therapy. When LP is difficult, the patient may endure multiple attempts, prolonged anesthesia time, and with failure of LP may require fluoroscopy-guidance with associated radiation exposure. This investigation will evaluate lumbar punctures performed in the intraoperative setting by oncologists with ultrasound guidance performed by the anesthesiologist in the leukemic pediatric population. The investigators hypothesis is that anesthesiologist guided ultrasound assistance will decrease intraoperative time, number of attempts and need to have the procedure done with fluoroscopy minimizing radiation exposure.

Primary Outcome

Number of punctures required to obtain cerebral spinal fluid.

Interventions

  • PROCEDURE Ultrasound

Trial Details

FieldValue
Enrollment Target 3 participants
Start Date 2012-07
Est. Completion 2014-05
Phase NA
Nationwide Children's Hospital

188 total trials

Why NCT01643291 stopped before completion

NCT01643291 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 3 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).

The record links to 0 conditions, and to 1 intervention - of which Ultrasound is the first listed.

NCT01643291 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01643291 about?

NCT01643291 is a clinical study titled "Ultrasound Use for Difficult Lumbar Punctures in Pediatric Oncology Patients". Hematology-oncology patients may require frequent lumbar puncture for diagnosis, assessment and therapy. When LP is difficult, the patient may endure multiple attempts, prolonged anesthesia time, and with failure of LP may require fluoroscopy-guidance with associated radiation exposure. This investi...

What is the current status of trial NCT01643291?

This trial is currently terminated. It is a NA study. The enrollment target is 3 participants. The study started on 2012-07. Estimated completion is 2014-05.

What interventions are being tested in trial NCT01643291?

The interventions under investigation include: Ultrasound (PROCEDURE).

Who is sponsoring clinical trial NCT01643291?

This trial is sponsored by Nationwide Children's Hospital, which has 188 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01643291's enrollment target sits among peer trials

3 1996th of 2000 higher than 4 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01643291, the US trial registry maintained by the National Library of Medicine. NCT01643291 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.