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Quick Needle-Free test could spot long COVID

NCT ID NCT07343856

Diagnosis Sponsor: Oncology Center,Ministry Of Heath,Uzbekistan Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only This study
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests a new, non-invasive diagnostic method for long COVID. Researchers will use a single-session bioelectrical assessment to detect patterns linked to viral persistence in 50 adults with long COVID. The goal is to see if this approach can reliably identify ongoing viral antigens without needles or drugs.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could provide a quick, non-invasive diagnostic tool for long COVID, helping identify persistent viral antigens.
What could go wrong
This is a very small, early-stage diagnostic study (50 participants) with no treatment. The method is experimental and may not prove reliable or generalizable.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 50 people

The number the study aims to enrol. It can still change while the study runs.

Started

Dec 2025

Expected to finish

Jan 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 75 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Age 18 years or older * History of confirmed SARS-CoV-2 infection * Persistent symptoms consistent with Long COVID lasting ≥12 weeks after acute infection * Ability to provide informed consent * Willingness to undergo non-invasive bioelectrical diagnostic assessment Exclusion Criteria: * Acute infectious disease at the time of enrollment * Severe uncontrolled medical or psychiatric conditions that may interfere with diagnostic assessment * Implanted electronic medical devices (e.g., pacemaker) * Pregnancy or breastfeeding * Inability to comply with study procedures

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Conditions

The condition(s) this trial relates to.

long COVID-19 primary dysautonomia

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Long COVID Post acute sequelae of SARS CoV 2 infection

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Research Institute of Virology

    Tashkent, 100194, Uzbekistan

More trials for these conditions

Other studies related to the condition(s) this trial covers.