deltatrials
Unknown EARLY_PHASE1 NCT04326036

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.

Updated 8 times since 2020 Last updated: Feb 21, 2023 Started: Mar 25, 2020 Primary completion: Aug 1, 2023 Completion: Jan 31, 2024

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
  1. Mar 2025 — Present [monthly]

    Unknown EARLY_PHASE1

    Status: Enrolling By InvitationUnknown

  2. Sep 2024 — Mar 2025 [monthly]

    Enrolling By Invitation EARLY_PHASE1

  3. Jul 2024 — Sep 2024 [monthly]

    Enrolling By Invitation EARLY_PHASE1

  4. Mar 2023 — Jul 2024 [monthly]

    Enrolling By Invitation EARLY_PHASE1

  5. Apr 2022 — Mar 2023 [monthly]

    Enrolling By Invitation EARLY_PHASE1

    Status: RecruitingEnrolling By Invitation

Show 3 earlier versions
  1. Jan 2021 — Apr 2022 [monthly]

    Recruiting EARLY_PHASE1

  2. Nov 2020 — Jan 2021 [monthly]

    Recruiting EARLY_PHASE1

    Status: Enrolling By InvitationRecruiting

  3. 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

Sponsor contact:
  • Black Tie Medical, Inc.
  • Robert W. Alexander, MD
Data source: Black Tie Medical, Inc.

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations

  • Stevensville, United States