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Enrolling by invitationNCT07909603Updated Nov 2, 2026

Head and Neck Cancer Strategies

An observational study in Head and Neck Cancer (H&N) and Thyroid Cancer, sponsored by Aarhus University Hospital. Enrolling by invitation at 1 site in Denmark. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-11-02.

Primary conditionThyroid NeoplasmsRegistry: Head and Neck NeoplasmsReclassifiedWhy we changed it
Registry
Head and Neck Neoplasms — the first condition term the registry derived for this study.
ClinicalTrials.gg
Thyroid Neoplasms
Why
  1. The study's listed conditions name Thyroid Neoplasms, a narrower term within Head and Neck Neoplasms.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Aarhus University Hospital · Observational

Updated Nov 2, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
1,500
Ages
18 Years and older
Sex
All
01

Study summary

The overall aim is to investigate whether genetic and other molecular markers can improve the diagnosis, assessment of treatment response, and detection of recurrence in patients with head and neck cancer. In the longer term, the project aims to contribute to more individualised treatment strategies for our patients.

The project will involve comprehensive analyses of tumour tissue and blood, including extensive genetic sequencing and other molecular profiling. Importantly, the research analyses will not have any implications for the clinical management or treatment of the individual patient included in the study.

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Conditions studied

  • Head and Neck Cancer (H&N)
  • Thyroid Cancer

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Keywords

  • head and neck cancer
  • thyroid cancer
  • molecular markers
  • genetics
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In context

Thyroid Neoplasms Reclassified

785 studies on the registry are indexed under Thyroid Neoplasms; 204 are open to participants now.

This study's planned enrollment of 1,500 is above the median of 178 across 241 observational studies indexed under Thyroid Neoplasms.

Browse Thyroid Neoplasms studies →

Lead sponsor

Aarhus University Hospital is the lead sponsor of 298 studies on the registry; 80 are open to participants now.

Compared within Thyroid Neoplasms, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Head and Neck Neoplasms. The counts are of registry records indexed under each term, refreshed daily. How we classify →

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients suspected of Head and neck cancer or thyroid cancer

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Tumor more than 1 cm in the head and neck and suspecion of cancer

Exclusion criteria

Exclusion Criteria:

  • Tumor too small to assure tissue for correct diangosis
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
1,500 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna
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What researchers measure

Primary outcomes

  1. Number of somatic variants in head- and neck cancer based on DNA sequencing data

    WGS on tumor tissue

    Time frame: At study inclusion (pretreatment)

  2. Number of RNA alterations in head- and neck cancer based on RNA sequencing data

    Total RNA sequencing in tumor tissue

    Time frame: At study inclusion (pretreatment)

  3. Prevalence of ctDNA in blood in head- and neck cancer patients before and after treatment

    WGS

    Time frame: At study inclusion (pretreatment), and during follow-up: 2, 6, 12, 18, 24 months after treatment

Secondary outcomes

  1. The prevalence of microbioma in tumor tissue of head and neck cancer

    Sequencing analysis of bacterial DNA

    Time frame: At study inclusion (pretreatment)

  2. Growth of tumormodels from head and neck cancer

    Tumormodels from tumor samples from head and neck cancer patient

    Time frame: At study inclusion (pretreatment)

  3. Microbioma in saliva

    Sequencing analysis of bacterial DNA

    Time frame: At study inclusion (pretreatment), and 2 months after treatment during follow-up

  4. Prohibition of growth of tumormodels from head and neck cancer due to phamacological inhibition: size of tumor

    Tumormodels from tumor samples from head and neck cancer patient

    Time frame: At study inclusion (pretreatment)

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Study locations

1 site
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References and documents

Individual participant data

Plan to share: Undecided — Due to patient confidentiality and compliance with Danish legislation

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Oct 2026 (actual). Primary completion is estimated for Jul 2033, 81 months after the start.

Of 103 non-industry observational studies under Thyroid Neoplasms, half reached primary completion within 71 months of starting (the median), counting those still running; a quarter within 24 and three quarters within 311. This study's planned 81 months is above that.

Counting every sponsor, half of 112 studies reached it within 63 months; a quarter within 26 and three quarters within 311.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 7, 2026
First posted
Nov 2, 2026
StartActual
Oct 1, 2026
Primary completionEst.
Jul 31, 2033
CompletionEst.
Jul 31, 2038
Last update
Nov 2, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 2, 2026
Show all 1 update
  1. Nov 2, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07909603
Responsible party
Sponsor
First posted
Nov 2, 2026
Start date
Oct 1, 2026
Primary completion
Jul 31, 2033 (estimated)
Completion
Jul 31, 2038 (estimated)
Last update
Nov 2, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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