Long COVID Diagnostic Reactivity Assesment Test

Sponsor
Oncology Center,Ministry Of Heath,Uzbekistan
Study ID
NCT07343856
Status
Enrolling By Invitation

Conditions

  • Long COVID
  • Post-Acute Sequelae of SARS-CoV-2 Infection

Eligibility Criteria

Sex
ALL
Age
18 Years - 75 Years
Healthy Volunteers
Not accepted

Interventions

  • Electrodiagnostic Bioelectrical Assessment — DIAGNOSTIC_TEST
    A non-invasive diagnostic procedure performed during a single session to assess bioelectrical response patterns associated with viral antigen persistence. Measurements are obtained using standardized bioelectrical assessment techniques without administration of any therapeutic agents or interventions.

Study Details

This study is a diagnostic clinical investigation designed to evaluate bioelectrical response patterns assessed by electro-acupuncture-based medicament testing. The method is used to identify individual bioelectrical reactivity associated with the presence and persistence of pathological factors and to assess patient-specific responses to tested medicinal substances. The study involves a single-session, non-invasive diagnostic procedure without administration of pharmacological treatment. The primary objective is the methodological evaluation of the diagnostic approach and the characterization of the detected bioelectrical response patterns in the studied population.

Key Dates

First listed
Jan 15, 2026
Start date
Dec 5, 2025
Status verified
Dec 2025
Primary completion
Dec 30, 2026
Completion
Jan 1, 2027

Study Design

Enrollment
50 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC

Arms

  • Experimental: Diagnostic Assesment Arm
    This single-arm study includes participants undergoing a non-invasive electrodiagnostic assessment to evaluate bioelectrical response patterns associated with viral antigen persistence. No therapeutic intervention is administered.

Primary Outcome Measure

Number of Participants With Bioelectrical Response Patterns Consistent With Viral Persistence [ Time Frame: At enrollment (single diagnostic session) ]

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