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SURVive: investigating new imaging criteria for non-operative treatment following neoadjuvant chemoradiation in rectal cancer patients

SURVive: investigating new imaging criteria for non-operative treatment following neoadjuvant chemoradiation in rectal cancer patients - Novel imaging criteria after neoadjuvant therapy rectal cancer.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON48971
Enrollment
20
Registered
2018-07-04
Start date
2018-07-10
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

Rectalcancer rectalcarcinoma

Interventions

None listed

Sponsors

Heelkunde
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients with rectal cancer who are eligible for treatment with neoadjuvant chemoradiation Patients treated in the LUMC, HMC, Alrijne or GHZ. Age 18 years and older; Willing to participate in all aspects of the study

Exclusion criteria

Exclusion criteria: Patients with rectal cancer, receiving chemoradiation as part of the TESAR trial Diabetes mellitus Claustrofobia (low dose benzodiazepines are allowed); Prior radiotherapy to the pelvis If female and fertile: signs and symptoms of pregnancy or a positive pregnancy test / breast-feeding (a formal negative pregnancy test is not obligatory); Presence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule Contraindications for Magnetic Resonance Imaging Patient has evidence of infection in the 14 days prior to the FDG-PET/CT scan localised to the lower abdomen, pelvic region, lower back, inguinal region; Inability to tolerate lying supine for the duration of an FDG-PET/CT examination (~30min)

Design outcomes

Primary

MeasureTime frame
Evaluation of the accuracy of the combination of clinical data, MRI and digital FDG-PET/CT for prediction of response to chemoradiation therapy.

Secondary

MeasureTime frame
NVT

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)