Protocol Design for Evaluating the Immunity of Bivalve Fluids From Anodonta Cygnea in SARS and COVID-19

NCT05054075 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2022-04-15

No results posted yet for this study

Summary

The present work proposes to find if a bio-active composite in the hemolymph or plasma of the freshwater bivalve Anodonta cygnea is able to offer immunity and specificity for meliorating the major symptoms in human SARS and COVID-19 lineage infection. The Methodology concerns in silico procedures using organic fluids from 54 bivalves (in very specific conditions) to evaluate their therapeutic effects in 6 voluntary SARS and COVID-19 infected persons with an integrative diagnosis by a computational Mora®Nova apparatus to access the basal and experimental human physiological parameters.

Conditions

  • Coronavirus Infections
  • Coronavirus Sars-Associated
  • SARS (Severe Acute Respiratory Syndrome)
  • COVID-19

Interventions

BIOLOGICAL

Marine liquid and fluids

Marine liquid and fluids extracted from freshwater bivalve of A. cygnea (under very specific conditions)

BIOLOGICAL

Impregnation

SARS / COVID-19 fluid/liquid - impregnation

BIOLOGICAL

Incubation

SARS / COVID-19 fluid-bivalve-incubation

BIOLOGICAL

Manipulation

Bivalve Manipulation - Stress inducing

BIOLOGICAL

Refrigeration

Refrigerated fluid to check for maintained response

Sponsors & Collaborators

  • Instituto Politécnico de Bragança

    collaborator OTHER
  • Universidade do Porto

    lead OTHER

Principal Investigators

  • Jorge P Machado, PhD · ICBAS - Instituto de Ciências Biomédicas Abel Salazar

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
14 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-10-01
Primary Completion
2022-10-31
Completion
2022-11-30

Countries

  • Portugal

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05054075 on ClinicalTrials.gov