NCT07633860

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
49

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Dec 2022

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

Study Start

First participant enrolled

December 1, 2022

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2025

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

May 28, 2026

Completed
11 days until next milestone

First Posted

Study publicly available on registry

June 8, 2026

Completed
Last Updated

June 10, 2026

Status Verified

June 1, 2026

Enrollment Period

3 years

First QC Date

May 28, 2026

Last Update Submit

June 7, 2026

Conditions

Keywords

HistopathologySellar MassClinical spectrum

Outcome Measures

Primary Outcomes (1)

  • Correlation between pre-operative radiological features and definitive histopathological diagnosis.

    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

Study Arms (1)

Patients with confirmed sellar masses

Patients withe age of 11 to 65, who was diagnosed with sellar mass using MRI, and get treated surgically

Procedure: Craniectomy

Interventions

CraniectomyPROCEDURE

Bicoronal vs. Pterional approach vs endoscopic

Patients with confirmed sellar masses

Eligibility Criteria

Age11 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

included all Patients presenting with sellar region masses from December 2022 to December 2025, at Neurosurgical department at TMGH

You may qualify if:

  • Radiologically confirmed sellar, suprasellar, or parasellar mass.
  • Surgical candidacy
  • Histopathological confirmation
  • Age ≥ 11 year

You may not qualify if:

  • Incomplete diagnostics
  • Recurrent disease
  • Primary metastatic disease.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Thawrh General Modern Hospital

Sanaa, 975, Yemen

Location

MeSH Terms

Interventions

Craniotomy

Intervention Hierarchy (Ancestors)

Neurosurgical ProceduresSurgical Procedures, Operative

Study Officials

  • Adnan Al- Awdi, Neurosurgical consultant

    Arabic Board of Neurosurgery MD

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
21 Days
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Neurosurgical resident

Study Record Dates

First Submitted

May 28, 2026

First Posted

June 8, 2026

Study Start

December 1, 2022

Primary Completion

December 1, 2025

Study Completion

December 1, 2025

Last Updated

June 10, 2026

Record last verified: 2026-06

Locations