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CompletedNCT07911761Updated Nov 6, 2026

Prophylactic Central Neck Dissection for Papillary Thyroid Carcinoma

An observational study in Central Neck Dissection and Papillary Thyroid Carcinoma, sponsored by Mansoura University. Completed at 1 site in Egypt. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2026-11-06.

Sponsored by Mansoura University · Observational

Updated Nov 6, 2026Newly registered1 site added+1 moreGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
100
Ages
18 Years to 60 Years
Sex
All
01

Study summary

This study designed to examine the utility of prophylactic central neck dissection (CND) in the management of papillary thyroid carcinoma (PTC), to assess the association between risk factors as gender, age at diagnosis, and size of the tumor with performing central lymph node (CLN) affection, and to assess operative time, intraoperative and postoperative adverse events of CLN neck dissection.

Read the detailed description

Thyroid cancer is the most common endocrine cancer, contributing to 1-2% of all new malignancies diagnosed yearly worldwide.

The majority of thyroid carcinomas originate from follicular epithelial cells and include well-differentiated papillary thyroid carcinomas, up to 80% of all thyroid malignancies and follicular thyroid carcinomas about 15% of all thyroid malignancies. Moreover, undifferentiated anaplastic thyroid carcinoma 1-2% of all thyroid cancers, which is the most aggressive thyroid malignancy, also develops from epithelial cells.

Some authors recommend routine central LN neck dissection (CND) in thyroid cancer to prevent a future recurrence, citing the high risk of positive lymph nodes, better outcomes, and a lower morbidity rate associated with this initial operation, whereas others maintain that this procedure increases the risk of injury to the parathyroid glands and recurrent laryngeal nerves, with no demonstrable benefits in terms of long-term survival.

02

Conditions studied

  • Central Neck Dissection
  • 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 100 is below the median of 200 across 66 observational studies indexed under Thyroid Cancer, Papillary.

Browse Thyroid Cancer, Papillary studies →

Lead sponsor

Mansoura University is the lead sponsor of 1,119 studies on the registry; 183 are open to participants now.

Of its 9 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
Sampling method
Non-probability sample

Study population

In this prospective follow-up study, 100 patients with papillary thyroid carcinoma was included.

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

  • Age from 18 to 60 years old.
  • Patient with papillary thyroid carcinoma.

Exclusion criteria

Exclusion Criteria:

  • Patients are unfit for surgery.
  • Recurrence of thyroid cancer.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
100 participants (actual)
Patient registry
No

Groups and cohorts

  • Study group

    Patients With Clinically Node-Negative Papillary Thyroid Carcinoma

    Procedure: Thyroidectomy

Interventions

  • ProcedureThyroidectomy

    Patients underwent total thyroidectomy with prophylactic bilateral central neck dissection.

06

What researchers measure

Primary outcomes

  1. Percentage of Participants With Histopathologically Confirmed Occult Central Lymph Node Metastasis

    Percentage of participants with clinically and radiologically node-negative papillary thyroid carcinoma who have metastasis detected by histopathological examination of central compartment lymph nodes removed during prophylactic bilateral central neck dissection.

    Time frame: 24 hours postoperatively

07

Study locations

1 site
  • Mansoura University
    Al Mansurah, Mansoura 42541, 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 after the end of study for one year.

Supporting information: Study protocol

Time frame: After the end of study for one year.

Access criteria: The data will be available upon a reasonable request from the corresponding author.

No publications or documents are linked to this record.

09

Timeline

2 registry updates since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from May 2023 to primary completion in May 2023, 0 months.

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

Registered
Oct 28, 2026
First posted
Nov 3, 2026
StartActual
May 1, 2023
Primary completionActual
May 1, 2023
CompletionActual
May 1, 2025
Last update
Nov 6, 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.
Sites
1 site added, 1 site removed
Show site
  • Mansoura University · Al Mansurah, Egypt
Show 1 removed
  • Mansoura University · Al Mansurah, Egypt
Nov 6, 2026
Registered
First appeared on the registry
Nov 3, 2026
Show all 2 updates
  1. Nov 6, 2026
    1 site added, 1 site removed
    Show site
    • Mansoura University · Al Mansurah, Egypt
    Show 1 removed
    • Mansoura University · Al Mansurah, Egypt
  2. Nov 3, 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
NCT07911761
Responsible party
Mohamed Reda Ismail (Resident of General Surgery, Faculty of Medicine, Mansoura University, AL Dakahlia, Egypt, Mansoura University) — Principal investigator
First posted
Nov 3, 2026
Start date
May 1, 2023
Primary completion
May 1, 2023
Completion
May 1, 2025
Last update
Nov 6, 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 Oct 2026. You cannot join it, but the record below documents what was studied.

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