Actively Recruiting
Assessment of the Efficacy of Stereotactic Intracavitary Instillation of 90yttrium Colloid for Treatment of Cystic Lesions of the Pituitary and Surrounding Areas
Led by David Clarke · Updated on 2026-02-20
40
Participants Needed
1
Research Sites
17 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
There is no clear agreement on the best way to treat cystic lesions in the pituitary and surrounding areas, which are rare and challenging to manage. Traditional treatments like surgery or radiation often cannot fully remove or treat the cyst wall without serious risks. This research evaluates the use of stereotactic intracavitary instillation of 90yttrium colloid as a possible treatment option for these cystic sellar and parasellar tumors, aiming to find a safer and effective approach. The experimental treatment involves inserting 90yttrium colloid directly into the cystic cavity of the tumor during surgery. The neurosurgeon will decide the specific surgical approach based on individual patient needs, which will be described in the surgical consent. This procedure is compared to standard surgical care, and patients are monitored closely after treatment. Participants will undergo surgery as part of standard care, followed by monitoring for cyst shrinkage at 12 months after treatment. Imaging with PET-CT will be used within three weeks of treatment to locate the 90yttrium colloid. Researchers will track clinical and radiological stability, neurological function, and tumor response throughout the study, which may last several years until 2031.
CONDITIONS
Brief Title
90Yttrium Colloid for the Treatment of Cystic Sellar/Parasellar Tumors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 17 years or older
- Diagnosed with cystic sellar, suprasellar, parasellar, or intrasellar masses by histology, cytology, or neuroimaging
- Tumor measurements or volume can be calculated
- Requires surgical intervention as determined by the treating neurosurgeon
- Managed in the Halifax Neuropituitary Program surgical clinic
- Willing to undergo surgery and provide informed surgical consent
- Willing to provide informed consent for study participation
You will not qualify if you...
- Neurosurgeon's assessment that surgery poses unacceptable operative risk
- Having a solid tumor (non-cystic)
- Pregnant or breastfeeding at time of surgical consent or surgery
- Hypersensitivity, allergies, or contraindication to 90yttrium colloid
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 week
Participants undergo surgical insertion of 90yttrium colloid into the cystic cavity, with surgical parameters determined by the treating neurosurgeon based on clinical expertise.
1 surgical visit and several post-operative visits
Duration - Single treatment during surgery
Participants receive stereotactic intracavitary instillation of 90yttrium colloid as part of the surgical treatment for cystic sellar/parasellar tumors.
Treatment occurs during surgical visit
Duration - Up to 12 months post-treatment
Participants are monitored for cyst shrinkage and localization of 90yttrium colloid by PET-CT imaging to assess treatment efficacy and safety.
Visits within 3 weeks post-treatment and follow-up visits up to 12 months
Trial Site Locations
Total: 1 location
1
Halifax Infirmary
Halifax, Nova Scotia, Canada, B3H 3A7
Actively Recruiting
Research Team
D
David B. Clarke, MDCM, PhD, FRCSC, DABNS, FACS
A
Andrea LO Hebb, PhD, RN
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
Frequently Asked Questions
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