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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00432146
Other study ID # 2005/117
Secondary ID
Status Completed
Phase N/A
First received February 5, 2007
Last updated October 17, 2008
Start date September 2005
Est. completion date September 2006

Study information

Verified date February 2007
Source Istanbul University
Contact n/a
Is FDA regulated No
Health authority Turkey: Ethics Committee
Study type Observational

Clinical Trial Summary

Context: Although some of endocrine surgeons administer Lugol's solution to decrease thyroid gland vascularity, there is still no agreement on its effectiveness.

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.


Description:

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. 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.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date September 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 14 Years to 61 Years
Eligibility Inclusion Criteria:

- Graves disease

Exclusion Criteria:

- Anticoagulant usage,

- Previous thyroid operation,

- Refused to participate in this study.

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Drug:
lugol's solution


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Istanbul University
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