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NCT03857321 · ClinicalTrials.gov registry record · Phase 2

Study of Nasal Insulin to Fight Forgetfulness - Device Study

A Phase 2 study, sponsored by Wake Forest University Health Sciences.

Completed
Registry status
Phase 2
Development phase
20
Enrollment target

NCT03857321: Completed Phase 2 study, sponsored by Wake Forest University Health Sciences.

NCT03857321 is a Phase 2 study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 20 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03857321, a Phase 2 study, has completed, sponsored by Wake Forest University Health Sciences.

COMPLETED
Registry status
Phase 2
Development phase
20 participants
Enrollment target

Study Summary

The SNIFF Device study will involve using a device to administer insulin through each participant's nose or intra-nasally. Insulin is a hormone that is produced in the body. It works by lowering levels of glucose (sugar) in the blood. This study is measuring how much insulin the device delivers. In addition, this study will look at the effects of insulin or placebo administered intra-nasally using a nebulizer-like device on memory, blood, and cerebral spinal fluid.

Primary Outcome

Levels of insulin in cerebrospinal fluid after being delivered with the device. This will help to determine the ability of an intranasal delivery device to increase levels of insulin in cerebrospinal fluid (CSF)

Interventions

  • OTHER Placebo
  • DRUG Insulin
  • DEVICE intranasal nebulizer-like device

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2019-04-12
Est. Completion 2019-09-30
Phase Phase 2
Wake Forest University Health Sciences

1,140 total trials

What the finished NCT03857321 record still lists

NCT03857321 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower).

The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.

NCT03857321 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03857321 about?

NCT03857321 is a clinical study titled "Study of Nasal Insulin to Fight Forgetfulness - Device Study". The SNIFF Device study will involve using a device to administer insulin through each participant's nose or intra-nasally. Insulin is a hormone that is produced in the body. It works by lowering levels of glucose (sugar) in the blood. This study is measuring how much insulin the device delivers. In ...

What is the current status of trial NCT03857321?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 20 participants. The study started on 2019-04-12. Estimated completion is 2019-09-30.

What interventions are being tested in trial NCT03857321?

The interventions under investigation include: Placebo (OTHER), Insulin (DRUG), intranasal nebulizer-like device (DEVICE).

Who is sponsoring clinical trial NCT03857321?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03857321's enrollment target sits among peer trials

20 1805th of 2000 higher than 107 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT03857321, the US trial registry maintained by the National Library of Medicine. NCT03857321 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.