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Search / Trial NCT06166030

IMMUNERECOV CONTRIBUTES TO IMPROVEMENT OF RESPIRATORY AND IMMUNOLOGICAL RESPONSE IN POST-COVID-19 PATIENTS.

Launched by FEDERAL UNIVERSITY OF SÃO PAULO · Dec 10, 2023

Trial Information

Current as of July 26, 2025

Recruiting

Keywords

Covid 19 Dietary Supplementation Inflammation Lung Function Muscle Strength Sars Co V 2

ClinConnect Summary

The clinical trial titled "IMMUNERECOV CONTRIBUTES TO IMPROVEMENT OF RESPIRATORY AND IMMUNOLOGICAL RESPONSE IN POST-COVID-19 PATIENTS" is looking at how a special nutritional supplement called ImmuneRecov® can help people who are experiencing lingering health issues after having COVID-19. Many patients struggle with problems like weakened lung function and muscle strength for months after their illness. This study aims to see if taking ImmuneRecov® for 30 days can improve these symptoms, helping participants breathe easier and regain strength.

To be eligible for this trial, participants need to have had a confirmed COVID-19 diagnosis that required hospitalization and must be classified as having moderate illness, which means they have signs of lung issues but are still able to breathe without extra oxygen. The trial is currently recruiting individuals aged 65 to 74, and both men and women can participate. Those who have been out of the hospital for more than 14 days or who have started exercising or taking other supplements are not eligible. Participants can expect to take the supplement for a month and help contribute to important research that could improve recovery for many others affected by Long COVID.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria: The inclusion criteria encompassed post-COVID-19 patients with a confirmed COVID-19 diagnosis through a positive RT-PCR test, who also required hospitalization, meeting the criteria for moderate severity classification as defined by the World Health Organization (WHO). In summary, according to the WHO, moderate illness is characterized by individuals who exhibit signs of lower respiratory disease during clinical assessment or imaging and maintain an oxygen saturation level (SpO2) of ≥94% while breathing room air at sea level.
  • Exclusion Criteria: Exclusion criteria included individuals discharged from the hospital for more than 14 days and those who initiated physical activity or began taking any dietary supplements or vitamins.

About Federal University Of São Paulo

The Federal University of São Paulo (Universidade Federal de São Paulo - UNIFESP) is a prestigious institution dedicated to advancing education, research, and healthcare in Brazil. Renowned for its commitment to innovation and excellence, UNIFESP plays a pivotal role in clinical research, focusing on a multidisciplinary approach to improve health outcomes. The university fosters collaboration among researchers, healthcare professionals, and community stakeholders, ensuring that clinical trials conducted under its auspices adhere to rigorous ethical standards and contribute valuable insights to the medical field. With a rich history of academic achievement and a strong emphasis on translational research, UNIFESP is a key player in the development of new therapies and medical interventions.

Locations

Sao Jose Dos Campos, Sao Paulo, Brazil

São José Dos Campos, Sp, Brazil

Patients applied

0 patients applied

Trial Officials

Rodolfo de Paula Vieira, BSc., MSc., PhD.

Principal Investigator

Federal University of São Paulo

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported