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Thank you for your interest in the ENCORE trial!

The clinical reporting form (CRF) consists of a limited amount of data regarding anesthesia, surgery and oncological treatment of patients with colon cancer. The following information regarding institutional volume and follow-up are required to assess eligibility of your study site.

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* 1. 1.     Regarding the Hospital

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* 2. Contact 

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* 3. Does your hospital treat more than 50 patients with colon cancer per year?

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* 4. Will you be able to report postoperative adverse events (postoperative complications) according to the Clavien-Dindo classification within 30 days after surgery?

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* 5. Will you be able to report the date of return to original residency after recovery from surgery ?

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* 6. Will you or your colleagues be able to report surgical outcomes (recurrence, death etc) after 3 years?

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* 7. Preferred anesthetic technique for colo-rectal cancer surgery (with or without epidural)

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* 8. Are Epidurals commonly used for open surgery for colorectal cancer ?

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* 9. Are neuraxial blocks (spinal or epidural) commonly used for laparoscopic/robot colorectal cancer surgery?

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* 10. Do you have a ERAS program (Enhanced Recovery After Surgery) ?

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* 11. Do you have a Prehabilitation program (improving cardiorespiratory function before surgery ?

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* 12. Do you use cardiopulmonary exercise testing (CPET) for risk stratification ? 

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* 13. What OTHER risk stratification tool do you use?

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* 14. Regarding your participation: Are you willing to be the Primary Investigator (PI) from your site?

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* 15. Regarding your participation : Would you like to be the National coordinator (NC) for your country?

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* 16. Do you recommend another institution/ hospital/ colleague to contact for participation in the ENCORE Study ? If yes, please provide their contact details.

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