- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01347606
Secured Thyroidectomy With Intraoperative Methylene Blue Using (bluethyroid)
May 3, 2011 updated by: SB Istanbul Education and Research Hospital
Prospective Randomized Technical Study
Thyroid surgery has potential risks.
Intraoperative organ (such as parathyroides) extraction and vascular or neural (such as recurrent nervus) injuries are most important ones.
This research is aim to prevention of these via intraoperative methylene blue using.
Study Overview
Status
Unknown
Conditions
Detailed Description
Thyroid surgery has potential risks.
Intraoperative organ (such as parathyroides) extraction and vascular or neural (such as recurrent nervus) injuries are most important ones.
This research is aim to prevention of these via intraoperative methylene blue using.
In the operation when thyroid lobes manipulated to medially, methylene blue will be sprayed to this area.
Dying patternes of tissues (thyroid tissue, oparathyroid tissues, arteries, venules and neural structures) will ensure to identification the tissues.
Study Type
Observational
Enrollment (Anticipated)
20
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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Istanbul, Turkey
- Recruiting
- Bezmialem Vakif University
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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 70 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
thyroidectomy indicated patients
Description
Inclusion Criteria:
- Thyroidectomy indicated patients
Exclusion Criteria:
- Recurrent disease
- Additional disease
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
- Time Perspectives: Prospective
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: erhan aysan, Assoc. Prof., Bezmialem Vakif University
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
January 1, 2010
Primary Completion (Actual)
January 1, 2011
Study Completion (Anticipated)
July 1, 2011
Study Registration Dates
First Submitted
May 3, 2011
First Submitted That Met QC Criteria
May 3, 2011
First Posted (Estimate)
May 4, 2011
Study Record Updates
Last Update Posted (Estimate)
May 4, 2011
Last Update Submitted That Met QC Criteria
May 3, 2011
Last Verified
January 1, 2010
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 4-Aysan
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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