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NCT05225220 · ClinicalTrials.gov registry record · NA

Multimodal Investigation of Post COVID-19 in Females

A NA study, sponsored by Casa Colina Hospital and Centers for Healthcare.

Completed
Registry status
NA
Development phase
25
Enrollment target

NCT05225220: Completed NA study, sponsored by Casa Colina Hospital and Centers for Healthcare.

NCT05225220 is a NA study that has completed, run by Casa Colina Hospital and Centers for Healthcare. The registered enrollment target is 25 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05225220, a NA study, has completed, sponsored by Casa Colina Hospital and Centers for Healthcare.

COMPLETED
Registry status
NA
Development phase
25 participants
Enrollment target

Study Summary

The purpose of this study is to investigate the effects of transcutaneous vagus nerve stimulation (t-VNS) on Long Covid symptoms in females and to identify factors influencing susceptibility and recovery-particularly in the cognitive domain, as over 80% of long-haulers experience "brain fog".

Primary Outcome

Flanker is a non-verbal NIH Toolbox Cognition Battery assessment that measures both a participant's attention and inhibitory control.

Interventions

  • DEVICE Parasym Device (of Parasym Ltd, UK) using Transcutaneous Vagus Nerve Stimulation (t-VNS)

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2022-03-01
Est. Completion 2023-01-06
Phase NA

What the finished NCT05225220 record still lists

NCT05225220 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 25 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which Parasym Device (of Parasym Ltd, UK) using Transcutaneous Vagus Nerve Stimulation (t-VNS) is the first listed.

NCT05225220 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05225220 about?

NCT05225220 is a clinical study titled "Multimodal Investigation of Post COVID-19 in Females". The purpose of this study is to investigate the effects of transcutaneous vagus nerve stimulation (t-VNS) on Long Covid symptoms in females and to identify factors influencing susceptibility and recovery-particularly in the cognitive domain, as over 80% of long-haulers experience "brain fog".

What is the current status of trial NCT05225220?

This trial is currently completed. It is a NA study. The enrollment target is 25 participants. The study started on 2022-03-01. Estimated completion is 2023-01-06.

What interventions are being tested in trial NCT05225220?

The interventions under investigation include: Parasym Device (of Parasym Ltd, UK) using Transcutaneous Vagus Nerve Stimulation (t-VNS) (DEVICE).

Who is sponsoring clinical trial NCT05225220?

This trial is sponsored by Casa Colina Hospital and Centers for Healthcare, which has 8 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05225220's enrollment target sits among peer trials

25 1712th of 2000 higher than 265 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 NCT05225220, the US trial registry maintained by the National Library of Medicine. NCT05225220 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.