Rapid autopsy program aims to unlock secrets of aggressive lung cancer
NCT ID NCT05889546
First seen Jul 14, 2026 · Last updated Jul 15, 2026 · Updated 1 time
Summary
This study aims to create a rapid autopsy program for people with small cell lung cancer (SCLC). Within 10 hours of death, researchers collect tumor and blood samples to study the disease's biology. The goal is to generate new cell lines and genetic data that could lead to better therapies for this aggressive cancer.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this program could provide high-quality tumor samples that help researchers understand why small cell lung cancer is so aggressive and how to develop better treatments.
- What could go wrong
- This is a small pilot study focused on feasibility, not a treatment trial. It may not yield enough usable tissue or lead directly to new therapies.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2022
- Expected to finish
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Dec 2031
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Any patient with active SCLC being seen at IUSCCC clinics.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. ≥ 18 years old at the time of informed consent 2. Written informed consent and HIPAA authorization for release of personal health information. 3. Active SCLC diagnosis.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
3 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Indiana University Melvin and Bren Simon Comprehensive Cancer Center
RECRUITINGIndianapolis, Indiana, 46202, United States
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Roudebush VA Medical Center
RECRUITINGIndianapolis, Indiana, 46202, United States
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Sidney and Lois Eskenazi Hospital
RECRUITINGIndianapolis, Indiana, 46202, United States
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Other studies related to the condition(s) this trial covers.
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- Can an oral drug that starves tumors help Hard-to-Treat cancers?