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NCT06166030: IRPC
IMMUNERECOV CONTRIBUTES TO IMPROVEMENT OF RESPIRATORY AND IMMUNOLOGICAL RESPONSE IN POST-COVID-19 PATIENTS.
Phase 3 trial testing Nutritional blend (ImmuneRecov). in Long Covid19 in 58 participants. Status unknown.
10 December 2024
Quick facts
| Lead sponsor | Federal University of São Paulo |
|---|---|
| Phase | Phase 3 |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 58 |
| Start date | 10 December 2023 |
| Primary completion | 10 December 2024 |
| Estimated completion | 15 December 2024 |
| Sites | 2 locations across Brazil |
Drugs / interventions tested
- Nutritional blend (ImmuneRecov).
Conditions studied
- Long Covid19 — all drugs for Long Covid19 →
- Dietary Supplements — all drugs for Dietary Supplements →
- Respiratory Tract Infections — all drugs for Respiratory Tract Infections →
- Inflammation — all drugs for Inflammation →
Sponsor
Federal University of São Paulo
Who can join
18 and older, any sex, with Long Covid19 or Dietary Supplements. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Background: COVID-19 left consequences in different organs from months to years requiring different types of rehabilitation. In fact, a severe loss in the lung function, and in the respiratory and peripheral muscle strength is commonly observed in post-COVID-19 patients. Objectives: Thus, the present study investigated whether 30 days of supplementation with a nutritional blend (ImmuneRecov®; composition: whey protein concentrate, astaxanthin, creatine, selenium, vitamin C, glutamic acid, tryptophan, magnesium) would help to minimize the respiratory (lung function) and muscular (respiratory and peripheral muscles) sequelae in post-COVID-19 patients.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Beyond Antivirals: Alternative Therapies for Long COVID.
Livieratos A, Gogos C, Akinosoglou K. · · 2024 · cited 8× · PMID 39599909 · DOI 10.3390/v16111795 -
Consecutive intrabronchial administration of Wharton's jelly-derived mesenchymal stromal cells in ECMO-supported pediatric patients with end-stage interstitial lung disease: a safety and feasibility study (CIBA method).
Dominguez-Pinilla N, González-Granado LI, Gonzaga A, López Diaz M, et al · · 2025 · cited 3× · PMID 40188166 · DOI 10.1186/s13287-025-04289-3
Verify or expand the search:
- PubMed search for NCT06166030
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Federal University of São Paulo trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06166030 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Federal University of São Paulo
- Last refreshed: 12 December 2023
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06166030.
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