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NCT06304623: SVFCOVID-19

SVF for Treating Pulmonary Fibrosis Post COVID-19

Completed Phase 1 Last updated 12 March 2024
What this trial tests

Phase 1 trial testing Autologous adipose-derived SVF IV administration in Pulmonary Fibrosis in 40 participants. Completed in 1 March 2024.

Timeline
5 May 2020
Primary endpoint
1 March 2024
1 March 2024

Quick facts

Lead sponsorMichael H Carstens
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment40
Start date5 May 2020
Primary completion1 March 2024
Estimated completion1 March 2024
Sites2 locations across Nicaragua

Drugs / interventions tested

Conditions studied

Sponsor

Michael H Carstens — full company profile →

Who can join

Adults 18 to 85, any sex, with Pulmonary Fibrosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

General description of the study This is a prospective, multicenter, expanded access interventional study of subjects recovered from COVID-19 pneumonia to assess their response to intravenous administration of adipose-derived autologous SVF. Primary objective The purpose of this study was to evaluate the safety of single intravenous injections of autologous adipose-derived SVF produced using the GID SVF-2 device system for the treatment of secondary respiratory distress associated with COVID-19. Secondary objective To evaluate the efficacy of the initial treatment with SVF IV.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Pulmonary Fibrosis

Currently open trials in the same condition.

Other Michael H Carstens trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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/NCT06304623.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing