Papillary Thyroid CancerNCT07584447
Clinical Utility of Preoperative Thyroid GuidePx® Testing
An observational study of Papillary Thyroid Cancer and Papillary Thyroid Carcinoma, run by University of Calgary.
Trial summary
The purpose of this study is to learn whether having Thyroid GuidePx® test results available before treatment may help patients with papillary thyroid cancer and doctors make better-informed treatment decisions. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Papillary Thyroid Cancer, Papillary Thyroid Carcinoma
- How many people
- 85 participants
- Where
- No sites listed yet
- Study dates
- Apr 2026to Apr 2029
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Patients newly diagnosed with papillary thyroid cancer (Bethesda V and VI cytology) with localized disease who can potentially be treated with lobectomy
Who may be able to join
- Patients aged 18 years or older at the time of enrollment
- English-speaking
- Bethesda V or VI cytology following FNA of a thyroid nodule (papillary thyroid cancer)
- Bethesda III or IV with ThyroSpec positive for BRAFV600E, TERT, rearrangements in BRAF, RET, NTRK1, NTRK3, RAS + TERT, RAS + EIF1AX, AKT1, PI3CA, CTNNB1, EGFR, rearrangements in ALK
- Tumor 1- 4cm in size
- No lymph node involvement on ultrasound
- No gross extrathyroidal extension on ultrasound
Who cannot join
- Prior thyroid operation
- Distant metastatic disease
- Personal history of thyroid cancer
- History of whole-body radiation exposure or radiation to the head and neck region
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
The purpose of this study is to learn whether having Thyroid GuidePx® test results available before treatment may help patients with papillary thyroid cancer and doctors make better-informed treatment decisions.
- Medical subject headings
- Thyroid Cancer, Papillary
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Thyroid GuidePx® Tested Cohort | Not described |
What is being measured
The primary outcome is the main question the study is designed to answer.
Decision impact
Decision impact is defined as any change in treatment decision based on the Thyroid GuidePx® test results, including changes in surgical approach, reduction of unnecessary treatments, and addition of recommended treatments. Decision impact is measured using study-specific clinician and patient questionnaires administered before and after test results are available. Clinician decision impact is assessed by comparing treatments considered prior to testing with treatments recommended after review of test results, as well as clinician agreement with the statement "The test helped to make a treatment decision" rated on a 5-point Likert scale. Patient decision impact is assessed by patient report of whether the test helped them make a treatment-related decision (Yes/No) and the degree to which the test contributed to their care.
A copy of the questionnaires can be uploaded as required (study document upload is currently disabled).
Measured: 18 months
Secondary outcomes (4)
Incidence of total thyroidectomies
Incidence of total thyroidectomy of the tested cohort will be compared to historical controls.
Measured: 18 months
Incidence of completion thyroidectomies
Incidence of completion thyroidectomy of the tested cohort will be compared to historical controls.
Measured: 18 months
Recurrence outcomes
Recurrence outcomes, including biochemical recurrence (i.e., thyroglobulin ≥ 1 ng/mL) and/or tumor recurrence confirmed by imaging (i.e., CT, Ultrasound, etc.) of the tested cohort will be compared to historical controls. In the tested cohort, recurrence outcomes will be compared in Type 3 PTC (high risk) to Type 1 and 2 PTC (low risk).
Measured: 36 months
Costs
Costs related to treatment and follow-up will be compared in the tested cohort will be compared to historical controls For the cost analysis, costs related to clinician visits, treatments and complications will be compared in the study cohort and historical controls.
Measured: 18 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 May 2026
- Study startApr 2026 (estimated)
- Primary completionApr 2028 (estimated)
- Study completionApr 2029 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (21)Papers the sponsor has linked to this study.
- Other trials for Papillary Thyroid CancerStudies of the same condition, open and under way.
- More trials run by University of CalgaryThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 85 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Calgary
- Sponsor type
- University, hospital or other
- Collaborators
- Qualisure Diagnostics Inc., University of Alberta
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07584447
- Sponsor's protocol ID
- HREBA.CC-25-0488
- Status last verified
- Jan 2026
- First submitted
- 13 Jan 2026
- Last updated
- 1 Jun 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Chan WWL, Chan S, Kwong DLW. Radioiodine Refractory Differentiated Thyroid Cancer. Methods Mol Biol. 2022;2534:243-257. doi: 10.1007/978-1-0716-2505-7_17.
PubMed 35670980Tuttle RM, Li D, Ridouani F. Percutaneous ablation of low-risk papillary thyroid cancer. Endocr Relat Cancer. 2023 Feb 11;30(3):e220244. doi: 10.1530/ERC-22-0244. Print 2023 Mar 1.
PubMed 36629393Pace-Asciak P, Russell JO, Tufano RP. The Treatment of Thyroid Cancer With Radiofrequency Ablation. Tech Vasc Interv Radiol. 2022 Jun;25(2):100825. doi: 10.1016/j.tvir.2022.100825. Epub 2022 Mar 10.
PubMed 35551804Yoon JH, Choi W, Park JY, Hong AR, Kim HK, Kang HC. Active Surveillance for Low-Risk Papillary Thyroid Carcinoma as an Acceptable Management Option with Additional Benefits: A Comprehensive Systematic Review. Endocrinol Metab (Seoul). 2024 Feb;39(1):152-163. doi: 10.3803/EnM.2023.1794. Epub 2024 Jan 22.
PubMed 38417830Zhang M, He X, Wu J, Xie F. Differences between physician and patient preferences for cancer treatments: a systematic review. BMC Cancer. 2023 Nov 18;23(1):1126. doi: 10.1186/s12885-023-11598-4.
PubMed 37980466Schumm MA, Shu ML, Kim J, Tseng CH, Zanocco K, Livhits MJ, Leung AM, Yeh MW, Sacks GD, Wu JX. Perception of risk and treatment decisions in the management of differentiated thyroid cancer. J Surg Oncol. 2022 Aug;126(2):247-256. doi: 10.1002/jso.26858. Epub 2022 Mar 22.
PubMed 35316538Chan S, Karamali K, Kolodziejczyk A, Oikonomou G, Watkinson J, Paleri V, Nixon I, Kim D. Systematic Review of Recurrence Rate after Hemithyroidectomy for Low-Risk Well-Differentiated Thyroid Cancer. Eur Thyroid J. 2020 Feb;9(2):73-84. doi: 10.1159/000504961. Epub 2020 Jan 28.
PubMed 32257956Craig S, Stretch C, Farshidfar F, Sheka D, Alabi N, Siddiqui A, Kopciuk K, Park YJ, Khalil M, Khan F, Harvey A, Bathe OF. A clinically useful and biologically informative genomic classifier for papillary thyroid cancer. Front Endocrinol (Lausanne). 2023 Sep 12;14:1220617. doi: 10.3389/fendo.2023.1220617. eCollection 2023.
PubMed 37772080Castagna MG, Maino F, Cipri C, Belardini V, Theodoropoulou A, Cevenini G, Pacini F. Delayed risk stratification, to include the response to initial treatment (surgery and radioiodine ablation), has better outcome predictivity in differentiated thyroid cancer patients. Eur J Endocrinol. 2011 Sep;165(3):441-6. doi: 10.1530/EJE-11-0466. Epub 2011 Jul 12.
PubMed 21750043Jin Y, Van Nostrand D, Cheng L, Liu M, Chen L. Radioiodine refractory differentiated thyroid cancer. Crit Rev Oncol Hematol. 2018 May;125:111-120. doi: 10.1016/j.critrevonc.2018.03.012. Epub 2018 Mar 22.
PubMed 29650270Craig SJ, Bysice AM, Nakoneshny SC, Pasieka JL, Chandarana SP. The Identification of Intraoperative Risk Factors Can Reduce, but Not Exclude, the Need for Completion Thyroidectomy in Low-Risk Papillary Thyroid Cancer Patients. Thyroid. 2020 Feb;30(2):222-228. doi: 10.1089/thy.2019.0274. Epub 2020 Jan 9.
PubMed 31813323Murthy SP, Balasubramanian D, Subramaniam N, Nair G, Babu MJC, Rathod PV, Thankappan K, Iyer S, Vijayan SN, Prasad C, Nair V. Prevalence of adverse pathological features in 1 to 4 cm low-risk differentiated thyroid carcinoma. Head Neck. 2018 Jun;40(6):1214-1218. doi: 10.1002/hed.25099. Epub 2018 Feb 8.
PubMed 29417654Kluijfhout WP, Pasternak JD, Lim J, Kwon JS, Vriens MR, Clark OH, Shen WT, Gosnell JE, Suh I, Duh QY. Frequency of High-Risk Characteristics Requiring Total Thyroidectomy for 1-4 cm Well-Differentiated Thyroid Cancer. Thyroid. 2016 Jun;26(6):820-4. doi: 10.1089/thy.2015.0495. Epub 2016 May 20.
PubMed 27083216Lang BH, Shek TW, Wan KY. The significance of unrecognized histological high-risk features on response to therapy in papillary thyroid carcinoma measuring 1-4 cm: implications for completion thyroidectomy following lobectomy. Clin Endocrinol (Oxf). 2017 Feb;86(2):236-242. doi: 10.1111/cen.13165. Epub 2016 Sep 1.
PubMed 27467318Dhir M, McCoy KL, Ohori NP, Adkisson CD, LeBeau SO, Carty SE, Yip L. Correct extent of thyroidectomy is poorly predicted preoperatively by the guidelines of the American Thyroid Association for low and intermediate risk thyroid cancers. Surgery. 2018 Jan;163(1):81-87. doi: 10.1016/j.surg.2017.04.029. Epub 2017 Nov 8.
PubMed 29128185
Study at a glance
From the registry record, last updated by the sponsor on 1 Jun 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Clinical Utility of Preoperative Thyroid GuidePx® Testing
- ClinicalTrials.gov ID
- NCT07584447
- Acronym / sponsor ID
- HREBA.CC-25-0488
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 85 participants (estimated)
- Lead sponsor
- University of CalgaryUniversity, hospital or other
- Collaborators
- Qualisure Diagnostics Inc., University of Alberta
- Study start
- Apr 2026 (estimated)
- Primary completion
- Apr 2028 (estimated)
- Study completion
- Apr 2029 (estimated)
- First posted
- 13 May 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to learn whether having Thyroid GuidePx® test results available before treatment may help patients with papillary thyroid cancer and doctors make better-informed treatment decisions.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Thyroid GuidePx® Tested Cohort | – | – |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patients newly diagnosed with papillary thyroid cancer (Bethesda V and VI cytology) with localized disease who can potentially be treated with lobectomy
Key inclusion criteria (7 listed)
- Patients aged 18 years or older at the time of enrollment
- English-speaking
- Bethesda V or VI cytology following FNA of a thyroid nodule (papillary thyroid cancer)
- Bethesda III or IV with ThyroSpec positive for BRAFV600E, TERT, rearrangements in BRAF, RET, NTRK1, NTRK3, RAS + TERT, RAS + EIF1AX, AKT1, PI3CA, CTNNB1, EGFR, rearrangements in ALK
- Tumor 1- 4cm in size
Key exclusion criteria (4 listed)
- Prior thyroid operation
- Distant metastatic disease
- Personal history of thyroid cancer
- History of whole-body radiation exposure or radiation to the head and neck region
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Decision impact
Time frame: 18 months
Decision impact is defined as any change in treatment decision based on the Thyroid GuidePx® test results, including changes in surgical approach, reduction of unnecessary treatments, and addition of recommended treatments. Decision impact is measured using study-specific clinician and patient questionnaires administered before and after test results are available. Clinician decision impact is assessed by comparing treatments considered prior to testing with treatments recommended after review of test results, as well as clinician agreement with the statement "The test helped to make a treatment decision" rated on a 5-point Likert scale. Patient decision impact is assessed by patient report of whether the test helped them make a treatment-related decision (Yes/No) and the degree to which the test contributed to their care. A copy of the questionnaires can be uploaded as required (study document upload is currently disabled).
4 secondary outcomes
Incidence of total thyroidectomies
Time frame: 18 months
Incidence of completion thyroidectomies
Time frame: 18 months
Recurrence outcomes
Time frame: 36 months
Costs
Time frame: 18 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 Jun 2026.
- Results publication: PubMed 35670980Chan WWL, Chan S, Kwong DLW. Radioiodine Refractory Differentiated Thyroid Cancer. Methods Mol Biol. 2022;2534:243-257. doi: 10.1007/978-1-0716-2505-7_17.
- Results publication: PubMed 36629393Tuttle RM, Li D, Ridouani F. Percutaneous ablation of low-risk papillary thyroid cancer. Endocr Relat Cancer. 2023 Feb 11;30(3):e220244. doi: 10.1530/ERC-22-0244. Print 2023 Mar 1.
- Results publication: PubMed 35551804Pace-Asciak P, Russell JO, Tufano RP. The Treatment of Thyroid Cancer With Radiofrequency Ablation. Tech Vasc Interv Radiol. 2022 Jun;25(2):100825. doi: 10.1016/j.tvir.2022.100825. Epub 2022 Mar 10.
- Results publication: PubMed 38417830Yoon JH, Choi W, Park JY, Hong AR, Kim HK, Kang HC. Active Surveillance for Low-Risk Papillary Thyroid Carcinoma as an Acceptable Management Option with Additional Benefits: A Comprehensive Systematic Review. Endocrinol Metab (Seoul). 2024 Feb;39(1):152-163. doi: 10.3803/EnM.2023.1794. Epub 2024 Jan 22.
- Results publication: PubMed 37980466Zhang M, He X, Wu J, Xie F. Differences between physician and patient preferences for cancer treatments: a systematic review. BMC Cancer. 2023 Nov 18;23(1):1126. doi: 10.1186/s12885-023-11598-4.
- Results publication: PubMed 35316538Schumm MA, Shu ML, Kim J, Tseng CH, Zanocco K, Livhits MJ, Leung AM, Yeh MW, Sacks GD, Wu JX. Perception of risk and treatment decisions in the management of differentiated thyroid cancer. J Surg Oncol. 2022 Aug;126(2):247-256. doi: 10.1002/jso.26858. Epub 2022 Mar 22.
- Results publication: PubMed 32257956Chan S, Karamali K, Kolodziejczyk A, Oikonomou G, Watkinson J, Paleri V, Nixon I, Kim D. Systematic Review of Recurrence Rate after Hemithyroidectomy for Low-Risk Well-Differentiated Thyroid Cancer. Eur Thyroid J. 2020 Feb;9(2):73-84. doi: 10.1159/000504961. Epub 2020 Jan 28.
- Results publication: PubMed 37772080Craig S, Stretch C, Farshidfar F, Sheka D, Alabi N, Siddiqui A, Kopciuk K, Park YJ, Khalil M, Khan F, Harvey A, Bathe OF. A clinically useful and biologically informative genomic classifier for papillary thyroid cancer. Front Endocrinol (Lausanne). 2023 Sep 12;14:1220617. doi: 10.3389/fendo.2023.1220617. eCollection 2023.
- Results publication: PubMed 21750043Castagna MG, Maino F, Cipri C, Belardini V, Theodoropoulou A, Cevenini G, Pacini F. Delayed risk stratification, to include the response to initial treatment (surgery and radioiodine ablation), has better outcome predictivity in differentiated thyroid cancer patients. Eur J Endocrinol. 2011 Sep;165(3):441-6. doi: 10.1530/EJE-11-0466. Epub 2011 Jul 12.
- Results publication: PubMed 29650270Jin Y, Van Nostrand D, Cheng L, Liu M, Chen L. Radioiodine refractory differentiated thyroid cancer. Crit Rev Oncol Hematol. 2018 May;125:111-120. doi: 10.1016/j.critrevonc.2018.03.012. Epub 2018 Mar 22.
- Results publication: PubMed 31813323Craig SJ, Bysice AM, Nakoneshny SC, Pasieka JL, Chandarana SP. The Identification of Intraoperative Risk Factors Can Reduce, but Not Exclude, the Need for Completion Thyroidectomy in Low-Risk Papillary Thyroid Cancer Patients. Thyroid. 2020 Feb;30(2):222-228. doi: 10.1089/thy.2019.0274. Epub 2020 Jan 9.
- Results publication: PubMed 29417654Murthy SP, Balasubramanian D, Subramaniam N, Nair G, Babu MJC, Rathod PV, Thankappan K, Iyer S, Vijayan SN, Prasad C, Nair V. Prevalence of adverse pathological features in 1 to 4 cm low-risk differentiated thyroid carcinoma. Head Neck. 2018 Jun;40(6):1214-1218. doi: 10.1002/hed.25099. Epub 2018 Feb 8.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Questions about this trial
What is this clinical trial studying?
An observational study of Papillary Thyroid Cancer and Papillary Thyroid Carcinoma, run by University of Calgary.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 1 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Elleine Allapitan (4032208440, elleine.allapitan@ucalgary.ca), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Decision impact (time frame: 18 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07584447, which also lists 21 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Jun 2026.