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The Protocol of Enhanced Recovery After Surgery in Colorectal Surgery (ERAS)

Fudan University logo

Fudan University

Status

Unknown

Conditions

Colorectal Surgery

Treatments

Procedure: enhanced recovery after surgery (ERAS) protocol
Procedure: control

Study type

Interventional

Funder types

Other

Identifiers

NCT00498290
2006-51

Details and patient eligibility

About

The purpose of this study is to determine whether ERAS is safe and can decrease surgical stress, increase functional recovery and reduce complication rate in colorectal surgery.

Full description

The key factors that keep a patient in hospital after uncomplicated major colorectal surgery include the need for parenteral analgesia(persistent pain), intravenous fluids (persistent gut dysfunction), and bed rest (persistent lack of mobility). These factors often overlap and interact to delay return of function. Obviously, postoperative complications will also prolong the time until recovery and ultimately length of stay. A clinical pathway, called Enhanced Recovery After Surgery(ERAS), to accelerate recovery after colonic resection based on a multimodal programme with optimal pain relief, stress reduction with regional anaesthesia, early enteral nutrition and early mobilisation has demonstrated improvements in physical performance, pulmonary function, body composition and a marked reduction of length of stay.

Comparison(s): A total of 500 cases colorectal surgery were randomized to receive ERAS protocol or the traditional protocol, such as mechanical bowl preparation, intravenous fluids until bowl movement recovery and bed rest.

Enrollment

500 estimated patients

Sex

All

Ages

20 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Colorectal surgery patients
  • Age 20~80
  • Without comorbidities which will influence prognosis, such as paralysis, spine cataface, or cardiac infarction

Exclusion criteria

  • Emergency
  • Combined other organ resection
  • Age > 80
  • Comorbidities which will influence prognosis, such as paralysis, spine cataface, or cardiac infarction

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

500 participants in 2 patient groups

A
Experimental group
Description:
received enhanced recovery after surgery (ERAS) protocol in colorectal surgery
Treatment:
Procedure: enhanced recovery after surgery (ERAS) protocol
B
No Intervention group
Description:
normal recovery protocol in colorectal surgery
Treatment:
Procedure: control

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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