Actively Recruiting

Age: 18Years +
All Genders
ID06913296

Do PTeye Score Correlate With Biochemical Markers in Parathyroid Adenoma?

Led by Aristotle University Of Thessaloniki · Updated on 2025-04-06

50

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying parathyroid adenoma patients to evaluate how the PTeye near-infrared autofluorescence device correlates with biochemical data during parathyroidectomy surgery. Identifying the parathyroid glands is essential for successful surgery, and this study aims to assess the usefulness of PTeye, a probe-based autofluorescence system, compared to biochemical markers. Patients undergoing typical open parathyroidectomy will have their parathyroid glands identified using the PTeye device. During surgery, the autofluorescence values recorded by the PTeye after gland recognition will be collected and analyzed. The study focuses on comparing these values with biochemical data collected intraoperatively and on the first day after surgery. Participants will be involved during their surgery when PTeye readings are taken, and biochemical tests will be done during and shortly after surgery. The main measurement is the correlation between PTeye values and biochemical markers related to parathyroid adenoma. This observational study does not involve additional treatment beyond standard surgery and monitors outcomes through routine biochemical assessments.

CONDITIONS

Brief Title

PTeye in Parathyroid Adenoma

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age over 18 years old
  • Diagnosis of primary hyperparathyroidism caused by adenoma
  • Patient has given informed consent
Not Eligible

You will not qualify if you...

  • Secondary and tertiary hyperparathyroidism
  • Re-operation for adenoma
  • Previous neck surgery
  • Patient enrolled in another study that may affect the results of this study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - 1 to 2 days

Participants undergo a typical open parathyroidectomy where parathyroid glands are identified using the PTeye autofluorescence device. Values from the device are recorded intraoperatively and on the first postoperative day.

Surgery day and 1 postoperative visit

Trial Site Locations

Total: 1 location

1

Aristotle Univeristy of Thessaloniki

Thessaloniki, Greece, 54636

Actively Recruiting

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Research Team

T

Theodossis Papavramidis, Professor of Surgery

A

Angeliki Chorti, Dr

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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