- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02113683
Validation of MMS Test for Cancer Monitoring (MMS-TM)
June 20, 2018 updated by: MedInnovation GmbH
Validation of MMS Test to Detect Active Tumor Growth of Different Cancer Types Before and After Therapy, as Well as for Subsequent Relapse Control in Comparison to Conventional Methods
The purpose of this study is the validation of MMS test to detect active tumor growth in different cancer types before and after therapy, as well as in the course of therapy and for subsequent relapse control compared to standard methods (clinical examination, imaging, tumor markers).
It should be consider whether the MMS test has comparable diagnostic accuracy, and thus can replace more expensive or invasive procedures in future.
Study Overview
Status
Terminated
Conditions
Study Type
Observational
Enrollment (Actual)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Berlin, Germany, 13125
- HELIOS Klinikum Berlin-Buch, Klinik für Interdisziplinäre Onkologie
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
patients with primary diagnosis of cancer
Description
Inclusion Criteria:
- Clinical diagnosis of colo-rectal cancer
- Clinical diagnosis of stomach cancer
- Suspected diagnosis of melanoma
Exclusion Criteria:
- Colitis ulcerosa
- Morbus Crohn
- Cancer in time period two years before
- Cancer therapy in time period two years before
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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MMS test
therapy monitoring of patients with colo-rectal or stomach disease or with melanoma
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
active tumor growth before and after cancer therapy
Time Frame: up to 36 month
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up to 36 month
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Katja Waterstradt, PhD, MedInnovation GmbH
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2014
Primary Completion (ACTUAL)
June 20, 2018
Study Completion (ACTUAL)
June 20, 2018
Study Registration Dates
First Submitted
April 8, 2014
First Submitted That Met QC Criteria
April 10, 2014
First Posted (ESTIMATE)
April 15, 2014
Study Record Updates
Last Update Posted (ACTUAL)
June 21, 2018
Last Update Submitted That Met QC Criteria
June 20, 2018
Last Verified
March 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Digestive System Diseases
- Neoplasms, Connective and Soft Tissue
- Neoplasms by Histologic Type
- Neoplasms
- Neoplasms by Site
- Gastrointestinal Neoplasms
- Digestive System Neoplasms
- Gastrointestinal Diseases
- Stomach Diseases
- Neuroectodermal Tumors
- Neoplasms, Germ Cell and Embryonal
- Neoplasms, Nerve Tissue
- Intestinal Diseases
- Intestinal Neoplasms
- Rectal Diseases
- Colorectal Neoplasms
- Neuroendocrine Tumors
- Nevi and Melanomas
- Sarcoma
- Stomach Neoplasms
- Rectal Neoplasms
- Melanoma
Other Study ID Numbers
- MMS-tm14
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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