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Genetic Examination of Patients With Primary Multiple Hernia

NCT00979095 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2010-10-13

No results posted yet for this study

Summary

The investigators are performing a genetic study of patients with multiple hernias (at least 3 primary hernias) versus a healthy control group. This genetic information is compared with circulating and subcutaneously biomarkers such as matrix-metalloproteinases (MMP's).

The hypothesis is that patients with multiple hernias have different expression of specific genes compared to the healthy control group.

Conditions

  • Multiple Hernia

Sponsors & Collaborators

  • Herlev Hospital

    lead OTHER

Principal Investigators

  • Jacob Rosenberg, Prof. MD · Herlev Hospital

  • Jakob Burcharth, MD · Herlev Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-06-30
Primary Completion
2011-06-30
Completion
2011-12-31

Countries

  • Denmark

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00979095 on ClinicalTrials.gov