- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01095341
Postoperative Hyperthyroidism
March 29, 2010 updated by: Heidelberg University
Postoperative Hyperthyroidism After Parathyroidectomy
The purpose of this study is to evaluate the frequency and the clinical course of postoperative hyperthyroidism following surgery of tertiary hyperparathyroidism (THP) and to determine the diagnostic value of thyroglobulin in this setting.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
57
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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Heidelberg, Germany, 69120
- University Hospital Heidelberg
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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 to 90 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
patients with tertiary hyperparathyroidism undergoing surgery for this reason
Description
Inclusion Criteria:
- patients with tertiary hyperparathyroidism undergoing surgery for this reason
- dialysis treatment
Exclusion Criteria:
- patients wish
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 |
Intervention / Treatment |
---|---|
THP
THP: patients undergoing parathyroidectomy according to tertiary hyperparathyroidism
|
|
Other causes
patients with hyperthyroidism not caused by parathyroidectomy
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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Hyperthyroidism
|
Secondary Outcome Measures
Outcome Measure |
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Thyroglobulin elevation
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Gottfried Rudofsky, MD, University Hospital Heidelberg Germany
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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
April 1, 2008
Primary Completion (Actual)
April 1, 2009
Study Completion (Actual)
April 1, 2009
Study Registration Dates
First Submitted
March 29, 2010
First Submitted That Met QC Criteria
March 29, 2010
First Posted (Estimate)
March 30, 2010
Study Record Updates
Last Update Posted (Estimate)
March 30, 2010
Last Update Submitted That Met QC Criteria
March 29, 2010
Last Verified
March 1, 2010
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- GR-2010
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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