CClinicalTrials.gg
Status unknownNCT05568641Updated Jan 18, 2023

Vitamin-D Receptor in Laryngeal Squamous Cell Carcinoma

An observational study in Laryngeal Carcinoma, sponsored by Sohag University. Status unknown. Open to participants aged 20 Years to 90 Years. Per ClinicalTrials.gov, last updated 2023-01-18.

Sponsored by Sohag University · Observational

The sponsor has not verified this record recently (last verified Jan 2023), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Other
Time perspective
Retrospective
Enrollment
50
Ages
20 Years to 90 Years
Sex
All
01

Study summary

Laryngeal squamous cell carcinoma (LSCC) is the second most common primary malignant tumor of the respiratory tract after lung cancer and the second most common primary epithelial malignant tumor of the head and neck. The age of onset of LSCC is mostly between 50 and 70 years, with a male to female ratio of approximately 4:1 .According to estimates by the American Cancer Society, in the United States, approximately 12,470 new cases of laryngeal cancer will be diagnosed and 3,820 people will die from laryngeal cancer in 2022.

The nuclear vitamin D receptor (VDR) is involved in multiple pathways that have many points of convergence. Some of these pathways are implicated in carcinogenesis thus the suggestion that VDR has a role to play in the biology of cancer [3]. Recent evidence indicates that the active form of vitamin D (1alpha, 25-dihydroxycholecalciferol) (VD) exhibits several different effects on normal and cancerous cells, including up-regulation of anti- proliferation and pro-apoptotic factors, as well as inhibition of cell-cycle promoters and growth factor signaling pathways. Thus it is useful as an anti-neoplastic agent in several human malignancies.

Studies in cell and animal model systems, as well as clinical trials have recognized the potential usefulness of VD and VD analogues as agents that enhance the anti-proliferative/cytotoxic effects of chemotherapy and ionizing radiation. Thus, at concentrations that produce limited hypercalcemia, these agents may be used as adjuncts to conventional chemotherapy and radiotherapy. We aim to analyze the expression of VDR in LSCC to determine potential for active VD therapy in such patients.

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Conditions studied

03

In context

Carcinoma

6,741 studies on the registry are indexed under Carcinoma; 1,161 are open to participants now.

This study's planned enrollment of 50 is below the median of 149 across 1,175 observational studies indexed under Carcinoma.

Browse Carcinoma studies →

Lead sponsor

Sohag University is the lead sponsor of 1,183 studies on the registry; 612 are open to participants now.

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

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Who can participate

Ages eligible
20 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

A retrospective study will be carried out on 50 LSCC specimens that were collected randomly from archives of Pathology Department, Faculty of Medicine, Sohag University

Inclusion criteria

  1. Both endoscopic and excisional biopsy specimens.
  2. All the studied cases include sufficient materials for the immunohistochemical study.
  3. Complete clinical data

Exclusion criteria

Exclusion Criteria:

  1. Patients with recurrence of the primary tumor.
  2. Patients with a history of preoperative chemotherapy and/or radiotherapy.
  3. Insufficient or tiny tissue biopsies
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Study design

Observational model
Other
Time perspective
Retrospective
Enrollment
50 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Diagnosis and prognosis of laryngeal squamous cell carcinoma

    Immunohistochemical Expression of Vitamin-D Receptor in Laryngeal Squamous Cell Carcinoma

    Time frame: Two or three days after staining tissue sections with Vit D receptor antibody

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: Undecided

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 Jan 18, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05568641
Lead sponsor
Sohag University
Responsible party
Amira Ahmed Abdelnaby (Lecturer of pathology, Sohag University) — Principal investigator
First posted
Oct 5, 2022
Start date
Jan 2023 (estimated)
Primary completion
Jan 2023 (estimated)
Completion
Mar 2023 (estimated)
Last update
Jan 18, 2023

Study contacts

Amira A Abdelnaby, Lecturer
Contact
ameraabdelnaby55@gmail.com
01002097612
Amira A Abdelnaby, Lecturer
principal investigator · Faculty of medicine ,Sohag university

Oversight

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

Not currently enrolling

This study is status unknown, as verified in Jan 2023. You cannot join it, but the record below documents what was studied.

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