Details
- Organisation Name: Cairns Hospital
- HHS: Cairns & Hinterland Hospital and Health Service
- Services Offered: Clinical Research Unit
- Website Address: www.health.qld.gov.au/services/cairns-hinterland/cairns_cairns_hosp
- Contact: Clinical Research Unit, Nurse Unit Manager- CairnsCRU@health.qld.gov.au
- Other Affiliated Research Sites: Townsville
Location
-16.9124 - 145.76831
Is your Facility able to initiate study activities prior to Ethics Committee protocol approval?
No
How long before Ethics Committee review is the Submission Packet required?
Greater than 2 weeks
Site Overview
The Clinical Research Unit (CRU) at the Cairns and Hinterland Hospital and Health Service (CHHHS) conducts clinical trials across several key areas:
Cardiology
Dermatology
Emergency Department
Intensive Care Unit (ICU)
Renal
Respiratory
Oncology
Teletrials
The CHHHS CRU is committed to advancing medical research and providing our patients and the community with early access to innovative therapies. Our unit supports researchers engaged in clinical trials that are commercially sponsored, externally initiated, or collaborative in nature, ensuring that our patients benefit from the latest advancements in medicine.
Our Mission
Early Access to Therapies: We strive to offer our patients early access to groundbreaking treatments and medical technologies through participation in clinical trials.
Advancing Medical Knowledge: By conducting clinical trials, we play a crucial role in expanding scientific knowledge and developing new standard treatments.
Rural and Remote Access: We collaborate with the Queensland Regional Clinical Trials Coordinating Centre (QRCCC) and other institutions, such as Townsville University Hospital, to provide teletrials that enable patients in rural and regional areas to access clinical trials.
This structured approach ensures our efforts are focused on enhancing patient care and expanding treatment options within our community.
Cardiology
Dermatology
Emergency Department
Intensive Care Unit (ICU)
Renal
Respiratory
Oncology
Teletrials
The CHHHS CRU is committed to advancing medical research and providing our patients and the community with early access to innovative therapies. Our unit supports researchers engaged in clinical trials that are commercially sponsored, externally initiated, or collaborative in nature, ensuring that our patients benefit from the latest advancements in medicine.
Our Mission
Early Access to Therapies: We strive to offer our patients early access to groundbreaking treatments and medical technologies through participation in clinical trials.
Advancing Medical Knowledge: By conducting clinical trials, we play a crucial role in expanding scientific knowledge and developing new standard treatments.
Rural and Remote Access: We collaborate with the Queensland Regional Clinical Trials Coordinating Centre (QRCCC) and other institutions, such as Townsville University Hospital, to provide teletrials that enable patients in rural and regional areas to access clinical trials.
This structured approach ensures our efforts are focused on enhancing patient care and expanding treatment options within our community.
HREC
- HREC Committee Name: Far North Queensland Human Research Ethics Committee
- Meeting frequency: Every 4 weeks
- Types of HREC (IRB/ERB/ETHICS) Committee that are used: Central Acting as Local
- Mandate distribution of safety: Yes
- Meeting frequency: Every 4 weeks
- Types of HREC (IRB/ERB/ETHICS) Committee that are used: Central Acting as Local
- Mandate distribution of safety: Yes
Facility staffing and training
- Handling Investigational Product: Yes
- Training program for the research staff: No
- Include GCP:
- Facility written sop during transportation to satellite site: N/A
- Training program for the research staff: No
- Include GCP:
- Facility written sop during transportation to satellite site: N/A
Licenses to receive, store, dispense and return controlled substances
- Required Licenses or Registrations: Yes
- Does the Facility have the ability to handle radio-labelled Investigational Products? No
- Does the Facility have the ability to handle radio-labelled Investigational Products? No
Equipment
- Investigational Product: Vertical laminar flow hood (chemo/hazardous drugs)
- Centrifuge: Yes
- Refrigerated Centrifuge: Yes
- Centrifuge: Yes
- Refrigerated Centrifuge: Yes
Patient Records
- Record Archiving:
- EMR/EHR systems: Other - ieMR
- Has your Clinical Trial Site or Service been accredited? Yes
- Audit Type: FDA ( Food Drug Administration), CRO ( Clinical Research Organisation), Sponsor
- EMR/EHR systems: Other - ieMR
- Has your Clinical Trial Site or Service been accredited? Yes
- Audit Type: FDA ( Food Drug Administration), CRO ( Clinical Research Organisation), Sponsor
Investigational product storage Capabilities
- Refrigerator (2 to 8 Degrees C): Yes
- Freezer (-20 to -30 Degrees C): Yes
- Investigational Freezer (-70 to -80 Degrees C): Yes
- Investigational Freezer (Liquid Nitrogen -135 Degrees C): No
- Does this equipment have back-up power? Yes
- Does this equipment provide Min/Max Temperature Monitoring? Yes
- Do you have the ability to generate a temperature monitoring log for this equipment? Yes
- Does this equipment have a temperature alarm? Yes
- Do you have an SOP which supports calibration of this equipment? Yes
- Freezer (-20 to -30 Degrees C): Yes
- Investigational Freezer (-70 to -80 Degrees C): Yes
- Investigational Freezer (Liquid Nitrogen -135 Degrees C): No
- Does this equipment have back-up power? Yes
- Does this equipment provide Min/Max Temperature Monitoring? Yes
- Do you have the ability to generate a temperature monitoring log for this equipment? Yes
- Does this equipment have a temperature alarm? Yes
- Do you have an SOP which supports calibration of this equipment? Yes
Specialty Research Area
Aboriginal and Torres Strait Islander
Study Types
Academic
Industry
Investigator
Source Document Types
Paper and Electronic
Average time to start study (in calendar days)
30-60
How long prior to HREC meeting does the application need to be submitted?
Greater than 2 weeks
Does the HREC committee require contract /budget approval prior to release final approval documents?
No
Does your Facility support in-patient admissions?
No
PK & PD specimens
Yes
Study Phase Capability
Device Pilot
Device Pivotal
Phase I
Phase II
Phase III
Phase IV
Type of Diagnostic Equipment
CT Scan Computerized Tomography Scan
DXA Dual-Energy X-ray Absorptiometry or Bone Densitometry
ECG/EKG Electrocardiogram
MAMMO Mammography
MRA Magnetic Resonance Angiography
MRI Magnetic Resonance Imaging
NMED Nuclear medicine e.g. Bone scan
PET Positron Emission Tomography Scan
Thallium cardiac stress test
Thyroid scan
X-Ray
Patient Population
Geriatrics 65 and onwards