NCT06550947

Brief Summary

  1. 1.Study the immunohistochemical expression of ALDOA in bladder urothelial cancer.
  2. 2.Correlate between ALDOA expression in specimens and different cilnicopathological factors.
  3. 3.Correlate between ALDOA expression and urothelial cancer prognosis and survival.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
50

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Sep 2024

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 9, 2024

Completed
4 days until next milestone

First Posted

Study publicly available on registry

August 13, 2024

Completed
19 days until next milestone

Study Start

First participant enrolled

September 1, 2024

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2025

Completed
Last Updated

August 13, 2024

Status Verified

August 1, 2024

Enrollment Period

10 months

First QC Date

August 9, 2024

Last Update Submit

August 9, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • Evaluate the immunohistochemical expression of ALDOA in bladder urothelial carcinoma.

    Microscopic examination of bladder urothelial carcinoma spicemens and staining them with ALDOA marker

    Baseline

Secondary Outcomes (1)

  • Evaluate relation between ALDOA expression and cilnicopathological features and patient survival.

    Baseline

Interventions

Immunohistochemical expression of ALDOA in bladder urothelial carcinoma

Eligibility Criteria

Sexall
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study will be conducted using formalin fixed paraffin embedded blocks of fifty cases of urothelial carcinomas . These blocks will be obtained from laboratory archives of the Pathology Department, Assiut University Hospital, Faculty of Medicine. Clinical data for this study will be obtained from laboratory archives of the pathology department, Assiut University Hospital, Assiut University.

You may qualify if:

  • All cases diagnosed as bladder urothelial cancer with known follow-up data and presence of muscle proper detected in the specimens.

You may not qualify if:

  • Subtypes of bladder cancer other than urothelial carcinoma subtype.
  • Cases of urothelial carcinoma without known follow up data.
  • Cases of urothelial carcinoma without muscle proper detected in the specimen.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Links

MeSH Terms

Interventions

Immunohistochemistry

Intervention Hierarchy (Ancestors)

HistocytochemistryCytological TechniquesClinical Laboratory TechniquesDiagnostic Techniques and ProceduresDiagnosisHistological TechniquesInvestigative TechniquesImmunologic Techniques

Study Officials

  • Dalia Elsers, Professor

    Head of Pathology Department

    STUDY DIRECTOR

Central Study Contacts

Merna Hesham John, Demonstrator

CONTACT

Heba Eldeek, Assistant professor

CONTACT

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Demonstrator

Study Record Dates

First Submitted

August 9, 2024

First Posted

August 13, 2024

Study Start

September 1, 2024

Primary Completion

July 1, 2025

Study Completion

August 1, 2025

Last Updated

August 13, 2024

Record last verified: 2024-08