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NCT06449365 · ClinicalTrials.gov registry record · Phase 4

Comparison of Intravenous V/S Nasal Atomizer Delivery of Midazolam for Conscious Sedation for No-scalpel Vasectomy

A Phase 4 study, sponsored by University of Tennessee Graduate School of Medicine.

Completed
Registry status
Phase 4
Development phase
35
Enrollment target

NCT06449365: Completed Phase 4 study, sponsored by University of Tennessee Graduate School of Medicine.

NCT06449365 is a Phase 4 study that has completed, run by University of Tennessee Graduate School of Medicine. The registered enrollment target is 35 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06449365, a Phase 4 study, has completed, sponsored by University of Tennessee Graduate School of Medicine.

COMPLETED
Registry status
Phase 4
Development phase
35 participants
Enrollment target

Study Summary

Purpose: This study compared administration of midazolam via intravenous route with nasal atomizer route for moderate sedation in an office-based vasectomy clinic.

Primary Outcome

comparison between groups

Interventions

  • DEVICE midazolam by nasal atomizer
  • DRUG intravenous midazolam

Trial Details

FieldValue
Enrollment Target 35 participants
Start Date 2017-10-22
Est. Completion 2020-08-07
Phase Phase 4

What the finished NCT06449365 record still lists

NCT06449365 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 35 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (93% lower).

The record links to 0 conditions, and to 2 interventions - of which midazolam by nasal atomizer is the first listed.

NCT06449365 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06449365 about?

NCT06449365 is a clinical study titled "Comparison of Intravenous V/S Nasal Atomizer Delivery of Midazolam for Conscious Sedation for No-scalpel Vasectomy". Purpose: This study compared administration of midazolam via intravenous route with nasal atomizer route for moderate sedation in an office-based vasectomy clinic.

What is the current status of trial NCT06449365?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 35 participants. The study started on 2017-10-22. Estimated completion is 2020-08-07.

What interventions are being tested in trial NCT06449365?

The interventions under investigation include: midazolam by nasal atomizer (DEVICE), intravenous midazolam (DRUG).

Who is sponsoring clinical trial NCT06449365?

This trial is sponsored by University of Tennessee Graduate School of Medicine, which has 20 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06449365's enrollment target sits among peer trials

35 1506th of 2000 higher than 481 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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 NCT06449365, the US trial registry maintained by the National Library of Medicine. NCT06449365 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.