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NCT Number: NCT07416149

Comparing PTeye-assisted Versus Conventional Total Thyroidectomy

This is a prospective, single-blinded, randomized controlled trial to evaluate whether PTeye™ can reduce post-operative hypoparathyroidism (PH). The study will enroll consecutive patients undergoing total thyroidectomy in a teritary endocrine surgery unit in Hong Kong, randomizing them into receiving conventional surgery versus PTeye™-assisted surgery. Subjects will be assigned to the two groups before surgery. Subjects will be under medical care as in usual practice.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Queen Mary Hospital

Hong Kong

Location status: Recruiting

Location contact

Man Him, Matrix Fung, MBBS

CONTACT

[email protected]

About this study

Post-operative hypoparathyroidism (PH) is a debilitating complication following total thyroidectomy. It arises from inadvertent removal or devascularization of the parathyroid glands. From a previous study in Hong Kong and other population-wide series, permanent PH rates could be as high as 11%, and transient PH rates being 30-48%, posing substantial burden on healthcare systems.

Near-infrared autofluorescence (NIRAF) technology has emerged to assist the identification and preservation of parathyroid glands during surgery. This study investigates the probe-based NIRAF device, PTeye™, which emits laser and receives NIR real-time, thereby detecting parathyroid glands by a simple touch of a probe.

A standardized protocol is devised to use PTeye™ for parathyroid identification at the early stage of surgery, in order to avoid devascularization or inadvertent removal of the parathyroids.

This is a prospective, single-blinded, randomized controlled trial to evaluate whether PTeye™ can reduce PH. The study will enroll consecutive patients undergoing total thyroidectomy in a tertiary endocrine surgery unit in Hong Kong. Patients will be randomized to receive conventional surgery or PTeye™-assisted surgery.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Adult patients ≥18 years of age
  • Undergoing total thyroidectomy, or completion total thyroidectomy
  • Pre-operative serum adjusted calcium levels within normal ranges

Exclusion criteria

  • Patients on pre-operative calcium or vitamin D supplements
  • Patients with pre-operative vitamin D deficiency, defined as serum vitamin D<30nmol/L
  • Patients with untreated primary or secondary hyperparathyroidism
  • Patient with known non-surgical hypoparathyroidism diseases
  • Patients with estimated glomerular filtration rate <30ml/1.73m2/min, on dialysis, or having a history of kidney transplant

Treatment and study plan

PTeye™ parathyroid detection system

Device

The PTeye™ parathyroid detection system is an adjunctive tool to aid in the identification of visually suspected parathyroid tissue as granted by DEN17005.

Primary outcomes

  1. Rate of significant post-operative hypoparathyroidism (SPH) after total thyroidectomy (in %)

    Time frame: 6 months

    Rate of significant post-operative hypoparathyroidism (SPH) after total thyroidectomy (in %)

Secondary outcomes

  1. Rate of inadvertent parathyroidectomy (in %)

    Time frame: within 4 weeks from operation

    Rate of inadvertent parathyroidectomy (in %)

  2. Rate of parathyroid auto-transplantation (in %)

    Time frame: within operation

    Rate of parathyroid auto-transplantation (in %)

  3. Day 0 PTH

    Time frame: Post-operative Day 0

    Day 0 Post-operative serum parathyroid hormone levels (pmol/L)

  4. Day 1 Post-operative serum parathyroid hormone levels (pmol/L)

    Time frame: Post-operative Day 1

    Day 1 Post-operative serum parathyroid hormone levels (pmol/L)

  5. 3-month Post-operative serum parathyroid hormone levels (pmol/L)

    Time frame: Post-operative 3 months

    3-month Post-operative serum parathyroid hormone levels (pmol/L)

  6. 6-month Post-operative serum parathyroid hormone levels (pmol/L)

    Time frame: Post-operative 6 months

    6-month Post-operative serum parathyroid hormone levels

Study contacts

Contact information is provided by the study sponsor or research team.

Man Him, Matrix Fung, MBBS

CONTACT

[email protected]

+852 2255 4232

Sponsors and collaborators

Lead sponsor

The University of Hong Kong

Other

Registry information

Official study title

Reducing Post-operative Hypoparathyroidism With Probe-based Near Infrared Autofluorescence (NIRAF)- Assisted Total Thyroidectomy Versus Conventional Total Thyroidectomy, a Randomized-controlled Trial

Important dates

Study start
2025
Primary completion
2028
Study completion
2028
First posted
Feb 17, 2026
Registry last updated
Feb 17, 2026

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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