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CompletedNCT07652450Thyroid cancerUpdated Aug 11, 2026

Incidental Thyroid Cancer in Cases With Inflammatory Thyroid Lesion

An interventional study of total thyroidectomy in Papillary Thyroid Cancer, Hashimoto Disease and Hashimoto's Thyroiditis, sponsored by Minia University. Completed at 1 site in Egypt. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2026-08-11.

Sponsored by Minia University · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 1 year 4 months after the study started (first participant enrolled Feb 2025, registered Jun 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
98
Allocation
Not applicable
Ages
18 Years to 60 Years
Sex
All
01

Study summary

This study aim to assess for the incidence of thyroid cancer in patients with autoimmune thyroiditis (Inflammatory thyroid Lesions)

Read the detailed description

The relationship between chronic inflammation and carcinogenesis is well established in multiple organ systems, including the liver, stomach, and colon. In the thyroid, chronic lymphocytic infiltration may create a pro-inflammatory microenvironment that promotes cellular proliferation, DNA damage, and oncogenic transformation. Several studies have suggested an increased risk of thyroid cancer, particularly papillary thyroid carcinoma (PTC), in patients with Hashimoto thyroiditis

02

Conditions studied

  • Papillary Thyroid Cancer
  • Hashimoto Disease
  • Hashimoto's Thyroiditis
  • Follicular Thyroid Cancer

Keywords

  • Incidental Thyroid Cancer
  • Autoimmune Thyroiditis
  • Hashimoto Thyroiditis
  • Differentiated Thyroid Cancer
  • Papillary Thyroid Carcinoma
03

In context

Thyroid Cancer, Papillary

186 studies on the registry are indexed under Thyroid Cancer, Papillary; 51 are open to participants now.

This study's enrollment of 98 is above the median of 41 across 114 interventional studies indexed under Thyroid Cancer, Papillary.

Browse Thyroid Cancer, Papillary studies →

Lead sponsor

Minia University is the lead sponsor of 370 studies on the registry; 117 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

  1. All types of thyroiditis, including:

    • Graves' disease
    • Toxic multinodular goiter (TMNG)
    • Toxic nodule (TN)
    • Hashimoto thyroiditis
    • Unspecified toxic nodular goiter
  2. Age between 18 and 60 years
  3. Underwent thyroid surgical operation (lobectomy or total thyroidectomy)

Exclusion criteria

Exclusion Criteria:

  1. Patients with known differentiated thyroid cancer before surgery
  2. Recurrent thyroid disease (previous thyroid surgery)
  3. Patients unfit for operation ( grade IV or V)
  4. Incomplete histopathological data
  5. Patients with medullary thyroid carcinoma or anaplastic thyroid cancer
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

ASA physical status

The anaesthetists’ scale of health before surgery: I is healthy, II has a mild illness that is under control, III a severe one, IV a severe illness that is a constant threat to life. V and VI are used for the critically ill and for organ donors.

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Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
98 participants (actual)

Study arms

  • Other
    Inflammatory thyroid lesions

    The presence of thyroiditis was determined considering histological diagnosis taken post-surgery, and we considered the correlation between any presence of thyroiditis and all Differentiated thyroid cancer, taken from the histopathological examination after pathologic analysis.

    Other: total thyroidectomy

Interventions

  • Othertotal thyroidectomy

    Diagnosis of differentiated thyroid cancer: The presence of thyroid cancer was determined based on histopathological examination of the resected specimen

06

What researchers measure

Primary outcomes

  1. • Incidence of incidental differentiated thyroid cancer with autoimmune thyroiditis

    Title: Incidence of incidental differentiated thyroid cancer Unit of measure: % of patients (proportion) Metric/method: Histopathological examination of surgical specimen

    Time frame: At time of surgery (postoperative histopathology)

Secondary outcomes

  1. Incidence of incidental differentiated thyroid cancer by autoimmune thyroiditis subtype

    Unit of Measure Percentage of patients within each subtype (Hashimoto thyroiditis, Graves' disease, toxic nodular goiter) Metric / Method Histopathological classification of thyroiditis subtype and cancer diagnosis; comparison using Chi-square test or Fisher's exact test

    Time frame: At time of surgery

  2. Outcome 3A: Age comparison

    Outcome Measure Title Mean age difference between patients with and without incidental differentiated thyroid cancer Unit of Measure Years (mean ± standard deviation) Metric / Method Unpaired Student's t-test or Mann-Whitney U test

    Time frame: At time of surgery

  3. Outcome 3B: Sex distribution

    Field Entry Outcome Measure Title Proportion of patients with positive anti-thyroid peroxidase (anti-TPO) antibodies who have incidental differentiated thyroid cancer Unit of Measure Percentage of patients Metric / Method Serological testing (anti-TPO antibodies measured by immunoassay); Chi-square test or logistic regression for association

    Time frame: Preoperative (within 30 days before surgery)

  4. Secondary Outcome 4 - Tumor characteristics Outcome 4A: Tumor size

    Outcome Measure Title Maximum tumor diameter in incidental differentiated thyroid cancers Unit of Measure Centimeters (mean ± standard deviation and range) Metric / Method Pathological measurement of surgical specimen

    Time frame: At time of surgery

  5. Outcome 4B: Microcarcinoma proportion

    Outcome Measure Title Proportion of incidental thyroid cancers that are microcarcinomas (≤1 cm) Unit of Measure Percentage of patients with incidental cancer Metric / Method Pathological measurement; defined as tumor size ≤1 cm

    Time frame: At time of surgery

  6. Outcome 4C: Lymph node metastasis

    Outcome Measure Title Proportion of patients with incidental differentiated thyroid cancer who have lymph node metastasis Unit of Measure Percentage of patients with incidental cancer Metric / Method Histopathological examination of central neck dissection specimens

    Time frame: At time of surgery

  7. Outcome 4D: Multifocality

    Outcome Measure Title Proportion of patients with incidental differentiated thyroid cancer who have multifocal disease Unit of Measure Percentage of patients with incidental cancer Metric / Method Histopathological examination (two or more distinct tumor foci)

    Time frame: At time of surgery

  8. Outcome 3E: Extrathyroidal extension

    Outcome Measure Title Proportion of patients with incidental differentiated thyroid cancer who have extrathyroidal extension Unit of Measure Percentage of patients with incidental cancer Metric / Method Histopathological examination (minimal or extensive extension)

    Time frame: At time of surgery

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Study locations

1 site
  • Faculty of medicine
    Minya, Minya Governorate 61611, Egypt
08

References and documents

Individual participant data

Plan to share: Yes — The data will be available upon a reasonable request from the corresponding author.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07652450
Lead sponsor
Minia University
Responsible party
Abdelrahman Mohamed Salah (Lecturer of General Surgery, Faculty of Medicine, Minia University, Minia, Egypt., Minia University) — Principal investigator
First posted
Jun 17, 2026
Start date
Feb 1, 2025
Primary completion
Feb 1, 2026
Completion
May 31, 2026
Last update
Aug 11, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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