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NCT05170425 · ClinicalTrials.gov registry record

LAMBDA 002 (Lung Registry) Study

A clinical trial of Lung Transplant Rejection, sponsored by Natera.

Active
Registry status
154
Enrollment target
11
Study locations

NCT05170425: Active study of Lung Transplant Rejection, sponsored by Natera.

NCT05170425 is a study of Lung Transplant Rejection that is active but no longer recruiting, run by Natera. The registered enrollment target is 154 participants, below the 635-participant average among 6 other Lung Transplant Rejection trials with a reported enrollment target (76% lower). The trial reports 11 study locations across 9 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05170425, a study of Lung Transplant Rejection, is active but no longer recruiting, sponsored by Natera.

ACTIVE NOT RECRUITING
Registry status
154 participants
Enrollment target
11
Study locations

Study Summary

The LAMBDA 002 registry study is an observational, longitudinal, multi-center study observing patients undergoing lung transplant.

Conditions Studied

Interventions

  • DEVICE Prospera

Study Locations (11)

Texas

  • UT Southwestern Medical Center - Dallas
  • Baylor College of Medicine Medical Center - Houston
  • Houston Methodist Hospital - Houston

California

  • Cedars-Sinai Medical Center - California City

Illinois

  • Northwestern Memorial Hospital - Chicago

Maryland

  • Johns Hopkins Hospital - Baltimore

Michigan

  • Corewell Health - Grand Rapids

Missouri

  • Washington University School of Medicine - St Louis

New York

  • Columbia University Irving Medical Center - New York

Ohio

  • Ohio State University Medical Center - Columbus

Trial Details

FieldValue
Enrollment Target 154 participants
Start Date 2022-11-04
Est. Completion 2027-05
Natera

27 total trials

What the registry record for NCT05170425 still lists

NCT05170425 is an observational study that tracks outcomes without assigning an intervention. The registered 154 participants enrollment target is mid-sized for trials with a published cap, below the 635-participant average among 6 other Lung Transplant Rejection trials with a reported enrollment target (76% lower).

The record links to 1 condition, with Lung Transplant Rejection appearing as the primary indexed condition, and to 1 intervention - of which Prospera is the first listed.

NCT05170425 lists 11 locations in 9 states (Texas, California, Illinois).

Frequently Asked Questions

What is clinical trial NCT05170425 about?

NCT05170425 is a clinical study titled "LAMBDA 002 (Lung Registry) Study". The LAMBDA 002 registry study is an observational, longitudinal, multi-center study observing patients undergoing lung transplant.

What is the current status of trial NCT05170425?

This trial is currently active not recruiting. The enrollment target is 154 participants. The study started on 2022-11-04. Estimated completion is 2027-05.

What conditions does trial NCT05170425 study?

This clinical trial studies the following conditions: Lung Transplant Rejection.

What interventions are being tested in trial NCT05170425?

The interventions under investigation include: Prospera (DEVICE).

Who is sponsoring clinical trial NCT05170425?

This trial is sponsored by Natera, which has 27 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05170425 being conducted?

This trial has 11 study locations across California, Illinois, Maryland, Michigan, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Lung Transplant Rejection

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

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Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

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Source: ClinicalTrials.gov NCT05170425, the US trial registry maintained by the National Library of Medicine. NCT05170425 (mid enrollment · multi site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.