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OpenTrials
Completed

NCT Number: NCT00571077

Electrical Impedance Scanning of Thyroid Nodules Prior to Thyroid Surgery: a Prospective Study

Patients over the age of 18 with thyroid nodules scheduled for surgery will undergo EIS scan. Each node will be scanned and graded form 1-5 (1=benign, 5=malignant). Results will be compared with final histopathology.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Hadassah-Hebrew University Medical Center, Jersualem, Israel

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients over the age of 18 with thyroid nodules scheduled for surgery.

Exclusion criteria

  • Pregnant patients
  • PAtients with electrical powered devices (cardiac pacemakers)

Treatment and study plan

Electrical Impedance Scanning (EIS) of the Thyroid gland

Device

Patients will be examined in the supine position. A cylinder electrode conveying 2.5V electrical current will be held by the patient. The patient will be scanned by a probe (similar to an ultrasound probe. The examination takes 5 minutes and there is no risk or discomfort.

Primary outcomes

  1. Sensitivity and specificity of EIS

    Time frame: 5 years

Secondary outcomes

  1. NPV and PPV of EIS of the thyroid

    Time frame: 5 years

Sponsors and collaborators

Lead sponsor

Hadassah Medical Organization

Other

Collaborators

  • Walter Reed Army Medical Center

Registry information

Important dates

Study start
2002
Study completion
2007
First posted
Dec 11, 2007
Registry last updated
May 13, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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