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NCT06023394 · ClinicalTrials.gov registry record · NA
Laryngeal Mask Airway in Laparoscopic Hernia Repair
A NA study, sponsored by Children's Mercy Hospital Kansas City.
- Completed
- Registry status
- NA
- Development phase
- 62
- Enrollment target
NCT06023394: Completed NA study, sponsored by Children's Mercy Hospital Kansas City.
NCT06023394 is a NA study that has completed, run by Children's Mercy Hospital Kansas City. The registered enrollment target is 62 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06023394, a NA study, has completed, sponsored by Children's Mercy Hospital Kansas City.
- COMPLETED
- Registry status
- NA
- Development phase
- 62 participants
- Enrollment target
Study Summary
This prospective randomized study will evaluate the effectiveness of laryngeal mask airway (LMA) versus endotracheal intubation (ETT) for patients undergoing laparoscopic inguinal hernia at CMH.
Primary Outcome
Oyxgen saturation will be measured by pulse oximetry in percent saturation at three time points during the anesthetic
Interventions
- DEVICE Laryngeal Mask Airway
- DEVICE Endotracheal Tube Device
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 62 participants |
| Start Date | 2023-03-27 |
| Est. Completion | 2024-05-08 |
| Phase | NA |
What the finished NCT06023394 record still lists
NCT06023394 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 62 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).
The record links to 0 conditions, and to 2 interventions - of which Laryngeal Mask Airway is the first listed.
NCT06023394 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT06023394 about?
NCT06023394 is a clinical study titled "Laryngeal Mask Airway in Laparoscopic Hernia Repair". This prospective randomized study will evaluate the effectiveness of laryngeal mask airway (LMA) versus endotracheal intubation (ETT) for patients undergoing laparoscopic inguinal hernia at CMH.
What is the current status of trial NCT06023394?
This trial is currently completed. It is a NA study. The enrollment target is 62 participants. The study started on 2023-03-27. Estimated completion is 2024-05-08.
What interventions are being tested in trial NCT06023394?
The interventions under investigation include: Laryngeal Mask Airway (DEVICE), Endotracheal Tube Device (DEVICE).
Who is sponsoring clinical trial NCT06023394?
This trial is sponsored by Children's Mercy Hospital Kansas City, which has 184 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT06023394's enrollment target sits among peer trials
62 1157th of 2000 higher than 837 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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