Effect of Lugol's Solution in the Patients With Graves' Disease
NCT ID: NCT00432146
Last Updated: 2008-10-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
36 participants
OBSERVATIONAL
2005-09-30
2006-09-30
Brief Summary
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Objective: The aims of this clinical trial are to evaluate thyroid blood flow and microvessel density in the patients with Graves' disease according to the Lugol's solution treatment preoperatively.
Design: Retrospective clinical trial. Setting: A tertiary referral center. Method: Thirty-six patients were randomly assigned to preoperative medication with Lugol's solution. Patients in group 1 (n=17) received Lugol's solution for 10 days before surgical intervention, whereas patients in group 2 (n=19) didn't receive it.
Main Outcome Measures: Blood flow through the thyroid arteries of patients with Graves' disease was measured by color flow Doppler ultrasonography. The microvessel density (MVD) was assessed immunohistochemically and Western blot analysis using the level of expression of CD-34 in thyroid tissue. The thyroid gland's weight and blood loss were measured in all patients.
Detailed Description
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Conditions
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Keywords
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Study Design
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PROSPECTIVE
Interventions
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lugol's solution
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Previous thyroid operation,
* Refused to participate in this study.
14 Years
61 Years
ALL
No
Sponsors
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Istanbul University
OTHER
Principal Investigators
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yesim erbil
Role: STUDY_DIRECTOR
Istanbul University
Other Identifiers
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2005/117
Identifier Type: -
Identifier Source: org_study_id