An observational, multicentre, non interventional programme to register patients diagnosed with neuroendocrine tumours (NETs) and monitor their patterns of care in Australian hospitals.

Neuroendocrine Tumour Non-interventional Patient Registry to monitor patterns of care in Australian Hospitals

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ANZCTR

Registry ID

ACTRN12609000805279

Acronym

SIGNETURe (Specialist Interest Group in Neuroendocrine Tumours Unique Registry)

Enrollment

500

Registered

2009-09-16

Start date

2009-10-01

Completion date

Unknown

Last updated

2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

This registry will enhance the national medical research effort for improved patient outcomes in Australia through improved diagnosis, reporting and management of NETs by collaboration among specialist oncologists, cancer registries and trialists at state and national levels.

Interventions

Non-interventional. This study will capture how patients are treated in current clinical practice. There will be no change to current clinical practice. The duration of the study is open-ended but analyses will be ongoing throughout the study period.

Eligibility

Sex/Gender

All

Age

0 to No maximum

Healthy volunteers

Inclusion criteria

Diagnosis of Neuroendocrine Tumour. Informed Consent Given.

Exclusion criteria

Nil

Outcome results