Barrett's esophagus (disorder)
Clinical Trial: AspECT
Year Started: 2005
AspECT: A Phase III, Randomised Study of Aspirin and Esomeprazole Chemoprevention in Barrett's Metaplasia. Trial has 10-year follow up period with samples collected throughout. Patient age groups given in the Sample Sets are the age of the patients at trial randomisation
- Access:
- Open to applicants
- Type:
- Clinical Trial
- Status:
- Completed
- Consent restrictions:
- Commercial restriction, DNA restriction
Associated Data Type | Procurement Timeframe |
---|---|
Followup records | 0 - 3 months |
Pathology records | 3 - 6 months |
Physiological/biochemical measurements | 0 - 3 months |
Treatment records | 0 - 3 months |
Female
Young adult (18 - 40 years)
11 - 100 donors
Material Type | Extraction Procedure | Storage Temperature | Preservation Type | Macroscopic Assessment | % of Sample Set |
---|---|---|---|---|---|
Tissue specimen | Surgical procedure (procedure) | RT | Paraffin | Affected | 51 - 75% |
Whole blood | -60°C to -85°C | N/A | Not applicable | 51 - 75% |
Malignant tumor of ovary (disorder)
Clinical Trial: 6MP
Year Started: 2011
See clinicaltrials.gov record NCT01432145 for more information about the study. Whole blood and plasma samples collected pre and post treatment in approx 70 participants and associated FFPE tumour tissue for approx 25 participants. Study data also available on request.
- Access:
- Open to applicants
- Type:
- Disease specific
- Status:
- Completed
- Consent restrictions:
- No restrictions
Associated Data Type | Procurement Timeframe |
---|---|
There is no associated data for this collection. |
Female
Adult (> 40 years)
11 - 100 donors
Material Type | Extraction Procedure | Storage Temperature | Preservation Type | Macroscopic Assessment | % of Sample Set |
---|---|---|---|---|---|
Plasma | -60°C to -85°C | N/A | Not applicable | 0 - 10% | |
Tissue specimen | Surgical procedure (procedure) | RT | N/A | Not applicable | 0 - 10% |
Whole blood | -60°C to -85°C | N/A | Not applicable | 0 - 10% |
Malignant tumor of ovary (disorder)
Clinical Trial: OCTOVA
Year Started: 2017
See ClinicalTrials.gov reference NCT03117933 for more information about the study. Whole blood and plasma samples pre and post-treatment with i.PARPi ii. control or iii. PARPi & anti-angiogenic. FFPE diagnostoc tumour sample.
- Access:
- Access restricted at present
- Type:
- Disease specific
- Status:
- In progress
- Consent restrictions:
- No restrictions
Associated Data Type | Procurement Timeframe |
---|---|
There is no associated data for this collection. |
Female
Adult (> 40 years)
11 - 100 donors
Material Type | Extraction Procedure | Storage Temperature | Preservation Type | Macroscopic Assessment | % of Sample Set |
---|---|---|---|---|---|
Plasma | -60°C to -85°C | N/A | Not applicable | 0 - 10% | |
Tissue specimen | Surgical procedure (procedure) | RT | N/A | Affected | 0 - 10% |
Whole blood | -60°C to -85°C | N/A | Not applicable | 0 - 10% |