Systematic Evaluation of Human Explant Model Systems Engineering (SEEDLING)
Study Overview
Status
Status
Conditions
Conditions
Detailed Description
Study Type
Study Type
Enrollment (Anticipated)
Enrollment
Contacts and Locations
Study Contact
Study Contact
- Name: Azaz Ahmed, Dr. med.
- Phone Number: +49-6221-56-7229
- Email: Azaz.Ahmed@med.uni-heidelberg.de
Study Contact Backup
- Name: Niels Halama, Dr. med.
- Phone Number: +49-6221-56-4801
- Email: Niels.Halama@nct-heidelberg.de
Study Locations
-
-
-
Heidelberg, Germany, 69120
- Recruiting
- University of Heidelberg / NCT
-
Contact:
- Azaz Ahmed, Dr. med.
- Phone Number: +49-6221-56-7229
- Email: Azaz.Ahmed@med.uni-heidelberg.de
-
Contact:
- Niels Halama, PD Dr. med
- Phone Number: +49 6221-56-7229
- Email: Niels.Halama@med.uni-heidelberg.de
-
Sub-Investigator:
- Anja Williams, Dr.
-
Sub-Investigator:
- Axel Benner
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Tissue material for Explant Model generation available or accessible
Exclusion Criteria:
- curatively resected/treated tumors
Study Plan
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Tissue Biopsy Specimen vs Tumor Explant Model Prediction
Time Frame: up to 24 weeks
|
Comparison of serial biopsy measurements to Explant Model measurements in the context of individual Patient variability, Serial biopsy timepoints can vary between 1 day up to 24 weeks
|
up to 24 weeks
|
Collaborators and Investigators
Sponsor
Sponsor
Collaborators
Collaborators
Investigators
Investigators
- Study Chair: Dirk Jaeger, Prof. Dr. med., University Hospital Heidelberg
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Anticipated)
Primary Completion
Study Completion (Anticipated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
Other Study ID Numbers
- U1111-1254-2831-S-507/2019
- U1111-1254-2831 (Other Identifier: World Health Organization (WHO))
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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