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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00865813
Other study ID # 1143/07
Secondary ID
Status Active, not recruiting
Phase N/A
First received March 18, 2009
Last updated March 18, 2009
Start date December 2008
Est. completion date December 2009

Study information

Verified date March 2009
Source University of Sao Paulo
Contact n/a
Is FDA regulated No
Health authority Brazil: Ethics Committee
Study type Interventional

Clinical Trial Summary

The purpose of this study was to identify accuracy rates of 2mm punch biopsy technique in diagnosing periocular malignancy.


Description:

In each case, the histology obtained at biopsy was compared with that identified at the time of tumor excision.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 40
Est. completion date December 2009
Est. primary completion date October 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- All lesions were initially examined at the slitlamp, after which lesions with malignant characteristics such as texture, size or color alterations asociated with ulceration, prominent borders or elevated contours, irregular borders, telangiectasias or loss of eyelashes were included.

Exclusion Criteria:

- Lesions with not malignant characteristics

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Procedure:
Punch Biopsy
Instillation of anesthetic eye drops. Asepsis Placement of surgical cloths and drapes Infiltration of the involved region with anesthetic solution plus adrenalin in1:200.00 dilution. Trephination of the most typical area of the lesion with a punch (2mm in diameter) of stainless steel by applying gentle pressure and twisting the trephine until its introduction into the suspicious lesions Removal of the excised tissue with the aid of an insulin needle or conjuntival forceps, the base then bein cut with an number 11 surgical blade

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Sao Paulo

Outcome

Type Measure Description Time frame Safety issue
Primary accuracy, positive predictive value, negative predictive value, sensitivity, specificity In each case, the histology obtained at biopsy was compared with that identified at the time of tumor excision. Yes
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