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. 2018 Jun 8;20(8):O226–O234. doi: 10.1111/codi.14257

Table 2.

Schedule of events

Event Baseline/Pre‐op Surgery 3–5 days postop 30 days postop 4–6 weeks postop 90 days postop 1 year postop (UK only)
Clinical assessments/investigations Clinical examination
Pre‐operative bloods
Operative details
Complications
Trial consent
Microbiome sub‐study (faecal samples)
Perfusion sub‐study (CTP and CTA) – OPTIONAL
Rectal contrast enema scan
Data collection time points Eligibility CRF
Baseline CRF
Operative CRF
30 days postsurgery f/up CRF
90 days postsurgery f/up CRF
1 year postsurgery f/up CRF a
Participant completed questionnaires EQ‐5D‐5L a
EORTC QLQ‐C30 and QLQ‐CR29 a
LARS
Resource use (UK sites only)

CRF, case report form; CTA, CT angiography; CTp, perfusion CT; f/up, follow‐up; LARS, low anterior resection syndrome; postop, postoperative; Pre‐op, preoperative.

a

Only required if this time point falls before the end of the planned follow‐up period (i.e. 90 days following the last participant's operation).