- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07633860
Sellar Masses: Clinical and Imaging Features With Correlation to Histopathology and Surgical Approach
Sellar, Supra-sellar and Para-sellar Region Masses: Clinical Spectrum and Imaging Features With Correlation to Histopathology and Surgical Approach: A Prospective Descriptive Study.
The goal of this observational study is to learn about the clinical spectrum of sellar masses, aiming to understand the correlation between the imaging features and the future surgical approach and histopathology results.
The main question it aims to answer is:
Does being both LMIC and conflict country change the global data!? Participants were included during a period of 3 years in a governmental hospital TMGH.
Study Overview
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Sanaa, Yemen, 975
- Thawrh General Modern Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Radiologically confirmed sellar, suprasellar, or parasellar mass.
- Surgical candidacy
- Histopathological confirmation
- Age ≥ 11 year
Exclusion Criteria:
- Incomplete diagnostics
- Recurrent disease
- Primary metastatic disease.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Patients with confirmed sellar masses
Patients withe age of 11 to 65, who was diagnosed with sellar mass using MRI, and get treated surgically
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Bicoronal vs. Pterional approach vs endoscopic
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Correlation between pre-operative radiological features and definitive histopathological diagnosis.
Time Frame: 3 years
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To evaluate the diagnostic accuracy of pre-operative magnetic resonance imaging (MRI) by determining the percentage of cases where pre-operative radiological features match the definitive post-operative histopathological classification (e.g., pituitary adenoma, craniopharyngioma, meningioma).
|
3 years
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Adnan Al- Awdi, Neurosurgical consultant, Arabic Board of Neurosurgery MD
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- TMGH-2026-Ethics-30
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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