Analyzing outcomes of endoscopic surgery for pituitary adenomas
Analysis of Operative Outcomes Following Endoscopic Resection of Pituitary Adenomas
This study is testing how well endoscopic surgery works for people with pituitary adenomas by looking at their vision, hormone levels, and overall recovery after the procedure.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 500 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | National Cheng-Kung University Hospital Academic / other |
| Locations | 1 site (Tainan) |
| Trial ID | NCT06156020 on ClinicalTrials.gov |
What this trial studies
This prospective study aims to evaluate the operative outcomes of patients with pituitary adenomas who undergo endoscopic endonasal resection. It focuses on assessing various outcomes, including visual, hormonal, survival, and functional results post-surgery. Data collected will include clinical history, laboratory results, radiographic images, and intraoperative videos for comprehensive analysis.
Who should consider this trial
Good fit: Ideal candidates for this study are adult patients diagnosed with pituitary adenomas who have undergone endoscopic endonasal resection.
Not a fit: Patients under 18 or over 80 years old, those with non-pituitary adenoma pathologies, or those who have had non-endoscopic surgery may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve understanding of the effectiveness and safety of endoscopic resection for pituitary adenomas, leading to better patient outcomes.
How similar studies have performed: Other studies have shown promising results with endoscopic approaches for pituitary adenomas, indicating potential for success in this study.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult patient * Pathological diagnosis of pituitary adenoma * Underwent endoscopic endonasal resection Exclusion Criteria: * Age \< 18 or \> 80 years * Non-pituitary adenoma pathologies * Underwent non-endoscopic surgery
Where this trial is running
Tainan
- National Cheng-Kung University Hospital — Tainan, Taiwan (Recruiting)
Study contacts
- Study coordinator: Jung-Shun Lee, MD
- Email: nslee1218@gmail.com
- Phone: +886-6-2353535
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.