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CompletedNCT07926633Updated Nov 10, 2026

Evaluation of Immunohistochemical Expression of Phosphohistone H3 (PHH3) in Meningioma

An observational study in Meningioma of Brain, sponsored by Sohag University. Completed at 1 site in Egypt. Per ClinicalTrials.gov, last updated 2026-11-10.

Sponsored by Sohag University · Observational

Updated Nov 9, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Case-only
Time perspective
Retrospective
Enrollment
50
Sex
All
01

Study summary

Evaluation of Immunohistochemical Expression of Phosphohistone H3 (PHH3) in Meningioma and associate its expression with certain clinical and pathological paramaters as age, sex of the patients, site (right or left and location), size, diagnosis, WHO grade, if there is bone invasion, if there is necrosis and vascular invasion.

Read the detailed description

Meningiomas are the most common primary central nervous system (CNS) tumors. Since the PHH3 was reported to be unique to mitosis, the anti-PHH3 antibody was being increasingly studied as a proliferation marker.

50 Specimens will be collected from Pathology Department of Sohag University Hospital. Sufficient clinical and histopathological data will be attached for each case.

The previously processed formalin-fixed, paraffin-embedded tissue blocks will be used to get Hematoxylin \& Eosin stained sections to confirm the diagnosis and to detect the histopathological type and grade of each tumor.

Another sliced tissue sections will be immunohistochemically stained with PHH3 monoclonal antibodies and assess its expression by counting positive mitotic nuclei. Correlation of PHH3 proliferative index with WHO histological grade and other clinicopathological parameters.

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Conditions studied

  • Meningioma of Brain

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Keywords

  • PHH3 Expression
  • Meningioma
  • Immunohistochemical study
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In context

Meningioma

255 studies on the registry are indexed under Meningioma; 85 are open to participants now.

This study's enrollment of 50 is below the median of 133 across 56 observational studies indexed under Meningioma.

Browse Meningioma studies →

Lead sponsor

Sohag University is the lead sponsor of 1,230 studies on the registry; 636 are open to participants now.

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

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Fifty (50) cases of meningioma will be performed from archieved formalin-fixed, paraffin-embedded tissue blocks referred to Pathology Department, Sohag University Hospitals.

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) confirmed meningioma cases. 2) Cases classified according to WHO CNS5 (2021). 3) Tissue blocks with sufficient material. 4) Specimens with sufficient clinical data.

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Exclusion criteria

Exclusion Criteria:

1) Tissue blocks with insufficient, destroyed or necrotic material. 2) Specimens with insufficient clinical data.

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Terms in these criteria, in plain language(1)

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.

Histologically or cytologically confirmed

The diagnosis was confirmed by looking at a sample under a microscope: tissue from a biopsy or surgery (histology), or cells from a fluid or needle sample (cytology).

Your pathology report is the document that shows this.

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Study design

Observational model
Case-only
Time perspective
Retrospective
Enrollment
50 participants (actual)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • Participants

    Fifty (50) cases of meningioma will be performed from archieved formalin-fixed, paraffin-embedded tissue blocks referred to Pathology Department, Sohag University Hospitals.

    Biological: Immunohistochemical staining

Interventions

  • BiologicalImmunohistochemical staining

    Immunohistochemical staining of paraffin embedded blocks of meningioma tissues by PHH3 monoclonal antibodies and assess its expression by counting positive mitotic nuclei. Correlation of PHH3 proliferative index with WHO histological grade and other clinicopathological parameters.

06

What researchers measure

Primary outcomes

  1. Evaluation of Immunohistochemical Expression of Phosphohistone H3 (PHH3) in Meningioma.

    PHH3 expression was evaluated by immunohistochemistry in meningioma specimens and scored according to the percentage of tumor cells showing positive nuclear staining. Expression was categorized into grade 1,2,3 for statistical analysis.

    Time frame: 6 months

Secondary outcomes

  1. Age

    Assessment of the association between PHH3 immunohistochemical expression and age subgroups

    Time frame: 6 months

  2. Sex

    Assessment of the association between PHH3 immunohistochemical expression and sex

    Time frame: 6 months

  3. Tumor site

    Assessment of the association between PHH3 immunohistochemical expression and tumor site

    Time frame: 6 months

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Study locations

1 site
  • Faculty of medicine Sohag university
    Sohag, Egypt
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References and documents

Individual participant data

Plan to share: Undecided — Not decided yet

No publications or documents are linked to this record.

09

Timeline

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

Ran from Sep 2026 to primary completion in Oct 2026, 1 month.

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

Registered
Oct 27, 2026
First posted
Nov 9, 2026
StartActual
Sep 1, 2026
Primary completionActual
Oct 1, 2026
CompletionActual
Oct 22, 2026
Last update
Nov 10, 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 9, 2026
Show all 2 updates
  1. Nov 10, 2026
    Minor edits only
    + 1 other change: verification date
  2. Nov 9, 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 ↗

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Registry details

Key details

Study ID
NCT07926633
Lead sponsor
Sohag University
Responsible party
Maria Adel Nagib (Demonstrator of pathology, Sohag University) — Principal investigator
First posted
Nov 9, 2026
Start date
Sep 1, 2026
Primary completion
Oct 1, 2026
Completion
Oct 22, 2026
Last update
Nov 10, 2026

Study contacts

Maisa Hashem Mohammed, Assistant professor
study director · Faculty of Medicine Sohag university

Oversight

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

Not currently enrolling

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

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Discussion

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