Actively Recruiting
90Yttrium Colloid for the Treatment of Cystic Sellar/Parasellar Tumors
Led by David Clarke · Updated on 2026-02-20
40
Participants Needed
1
Research Sites
908 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
There is no consensus in the literature on the best way to treat cystic lesions of the pituitary area. Patients who are symptomatic from these tumours are rare. The cystic form of tumours present special challenges since traditional treatment modalities (surgery and/or external radiation) are often not able to completely remove or treat the cyst wall without major morbidity or even mortality. There is no 'best practice' for the treatment of cystic tumours per se. Treatments available to patients with cystic sellar/parasellar tumours include conservative management using a 'wait and scan' approach, cyst drainage, and cyst removal via transsphenoidal and/or craniotomy approach (i.e. open surgery). Over the last 10 years we have treated approximately 8 patients with intracystic radiotherapy. All of these patients continue to be monitored clinically and radiologically and all have done well with stable regression of the cysts and no new neurological deficits. Over the past 2 years, 90yttrium colloid has been provided to CDHA through Health Canada's Special Access Program (SAP). It has only been of recent that Health Canada has requested a clinical trial to assess the benefit of intracystic radiotherapy over other available treatment options. The experimental treatment being proposed is the stereotactic intracavitary instillation of 90yttrium colloid for treatment of cystic lesions of the pituitary (sellar) and surrounding areas (parasellar).
CONDITIONS
Official Title
90Yttrium Colloid for the Treatment of Cystic Sellar/Parasellar Tumors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients 17 years of age or older
- Diagnosis of cystic sellar, suprasellar, parasellar, or intrasellar mass by histology, cytology, or neuroimaging
- Ability to measure tumor size or volume
- Requires surgical intervention as determined by the 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 considers surgery to have unacceptable operative risk
- Presence of a solid tumor instead of a cystic lesion
- Pregnant or breastfeeding at time of surgical consent or surgery
- Known allergy or contraindication to 90yttrium colloid radiopharmaceutical agent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
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
CONTACT
A
Andrea LO Hebb, PhD, RN
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here