Use of cSVF Via IV Deployment for Residual Lung Damage After Symptomatic COVID-19 Infection
Use of cSVF For Residual Lung Damage (COPD/Fibrotic Lung Disease After Symptomatic COVID-19 Infection For Residual Pulmonary Injury or Post-Adult Respiratory Distress Syndrome Following Viral (SARS-Co-2) Infection
Sponsor: Black Tie Medical, Inc.
This EARLY_PHASE1 trial investigates COPD and Coronavirus Infection and is currently ongoing. Black Tie Medical, Inc. leads this study, which shows 8 recorded versions since 2020 — indicating limited longitudinal coverage. Longitudinal tracking of infectious disease trials helps identify durability of treatment effects.
Change History
8 versions recorded-
Mar 2025 — Present [monthly]
Unknown EARLY_PHASE1
Status: Enrolling By Invitation → Unknown
-
Sep 2024 — Mar 2025 [monthly]
Enrolling By Invitation EARLY_PHASE1
-
Jul 2024 — Sep 2024 [monthly]
Enrolling By Invitation EARLY_PHASE1
-
Mar 2023 — Jul 2024 [monthly]
Enrolling By Invitation EARLY_PHASE1
-
Apr 2022 — Mar 2023 [monthly]
Enrolling By Invitation EARLY_PHASE1
Status: Recruiting → Enrolling By Invitation
▶ Show 3 earlier versions
-
Jan 2021 — Apr 2022 [monthly]
Recruiting EARLY_PHASE1
-
Nov 2020 — Jan 2021 [monthly]
Recruiting EARLY_PHASE1
Status: Enrolling By Invitation → Recruiting
-
Apr 2020 — Nov 2020 [monthly]
Enrolling By Invitation EARLY_PHASE1
First recorded
Mar 2020
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Black Tie Medical, Inc.
- Robert W. Alexander, MD
For direct contact, visit the study record on ClinicalTrials.gov .
Study Locations
- • Stevensville, United States