Actively Recruiting

Phase 3
Age: 17Years +
All Genders
NCT02081768

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

Age: 17Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Halifax Infirmary

Halifax, Nova Scotia, Canada, B3H 3A7

Actively Recruiting

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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

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