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NCT03263897 · ClinicalTrials.gov registry record · NA

Feasibility of Using a Mobile Device Controlled Micro-pressure Pulse Insufflator for Acute Migraine Relief

A NA study, sponsored by Caps Research Network.

Terminated
Registry status
NA
Development phase
59
Enrollment target

NCT03263897: Clinical Trial NA study, sponsored by Caps Research Network.

NCT03263897 is a NA study that was terminated before completion, run by Caps Research Network. The registered enrollment target is 59 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.

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The verdict

NCT03263897, a NA study, was terminated before completion, sponsored by Caps Research Network.

TERMINATED
Registry status
NA
Development phase
59 participants
Enrollment target

Study Summary

Evaluate the feasibility of using a mobile interface to control the insufflator device administering treatment for aborting (stopping) an acute episode of migraine. The patient, under clinical supervision, will use the mobile interface to "self administer" the treatment when experiencing an acute episode of migraine. The supervising clinician will monitor the patient and the device to make sure that no harm could come to the patient and will be ready to intervene if any adverse effects were suspected to or in the process of happening.

Primary Outcome

Subjects will grade the severity of their symptoms on a scale from 0 to 10. Changes in the symptoms severity scale will be assessed between pre and immediately post treatment

Interventions

  • DEVICE insufflation
  • DEVICE placebo insufflation

Trial Details

FieldValue
Enrollment Target 59 participants
Start Date 2017-08-21
Est. Completion 2020-12-31
Phase NA
Caps Research Network

3 total trials

Why NCT03263897 stopped before completion

NCT03263897 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 59 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 insufflation is the first listed.

NCT03263897 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03263897 about?

NCT03263897 is a clinical study titled "Feasibility of Using a Mobile Device Controlled Micro-pressure Pulse Insufflator for Acute Migraine Relief". Evaluate the feasibility of using a mobile interface to control the insufflator device administering treatment for aborting (stopping) an acute episode of migraine. The patient, under clinical supervision, will use the mobile interface to "self administer" the treatment when experiencing an acute ep...

What is the current status of trial NCT03263897?

This trial is currently terminated. It is a NA study. The enrollment target is 59 participants. The study started on 2017-08-21. Estimated completion is 2020-12-31.

What interventions are being tested in trial NCT03263897?

The interventions under investigation include: insufflation (DEVICE), placebo insufflation (DEVICE).

Who is sponsoring clinical trial NCT03263897?

This trial is sponsored by Caps Research Network, which has 3 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03263897's enrollment target sits among peer trials

59 1256th of 2000 higher than 745 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 NCT03263897, the US trial registry maintained by the National Library of Medicine. NCT03263897 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.