Rare Cystic Benign Adrenal Incidentalomas
Complex Cystic Benign Adrenal Incidentalomas Mimicking Non-adenomatous Masses; Rare Pathologies: Clinical Features and Outcomes. Case Series With Short Review of Literature.
1 other identifier
observational
291
1 country
1
Brief Summary
Benign complex cystic and vascular adrenal tumors comprise a group of lesions characterized by significant rarity. But, their detection is increasing due to improved radiologic imaging techniques. Nevertheless, they are still conflicting with other lesions. the investigators reviewed their experience with complex cystic benign adrenal tumors in adults, review previous reports to determine the appropriate diagnosis and management of these tumors.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2018
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 28, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 30, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2018
CompletedFirst Submitted
Initial submission to the registry
November 8, 2018
CompletedFirst Posted
Study publicly available on registry
November 14, 2018
CompletedNovember 14, 2018
November 1, 2018
3 months
November 8, 2018
November 9, 2018
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Number of patients with rare pathologies and correlation with demographic and radiological data
collection of rare pathologies ,correlation with other review of literature
7 years
Study Arms (1)
patients with adrenal masses
patients with adrenal mass managed by adrenalectomy
Eligibility Criteria
291 cases diagnosed with adrenal tumors were treated. Demographic criteria of studied cases and different types of pathologies identified . Three cases were diagnosed to have rare cystic and vascular histopathological variant including: cavernous haemangioma, capillary haemangioma and adrenal teratoma.
You may qualify if:
- cases with adrenal tumors above 18 years old with rare histopathology
You may not qualify if:
- age less than 18 years
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Urology and Nephrology Center
Al Mansurah, Aldakahlia, 35516, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- principal investigator
Study Record Dates
First Submitted
November 8, 2018
First Posted
November 14, 2018
Study Start
February 28, 2018
Primary Completion
May 30, 2018
Study Completion
June 30, 2018
Last Updated
November 14, 2018
Record last verified: 2018-11