CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 40 enrolled
Drug / intervention
Autologous adipose-derived SVF IV administrationbiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06304623
NCT06304623Phase 1Completed

The Role of Cellular Therapy With SVF Cells (Stromal Vascular Fraction) of Adipose Tissue Origin in the Treatment of Pulmonary Fibrosis Post COVD-19

Michael H Carstens·interventional·Posted Mar 12, 2024·Updated Mar 12, 2024

In Brief

A Phase 1 clinical trial evaluating Autologous adipose-derived SVF IV administration for Pulmonary Fibrosis. Completed, enrolled 40 participants across 2 sites.

Detailed Summary

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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesNicaragua

Timeline

Phase 1CompletedFinished
202120222023202420252026
First PostedMar 12, 2024
Enrollment StartMay 5, 2020
Primary CompletionMar 1, 2024
TodayJul 2, 2026
Enrollment to primary: 3.8 yearsPosted 2.3 years ago

Interventions

Autologous adipose-derived SVF IV administrationbiological

Subjects received an intravenous injection of autologous adipose-derived SVF.