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Implementation of Enhanced Recovery After Surgery Program (ERAS) in Colorectal Cancer Surgery, a Randomized Controlled Trial

A

Assiut University

Status

Completed

Conditions

Cancer of Colon

Treatments

Procedure: enhanced recovery after surgery program in colorectal cancer surgery

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of our study is to determine the effect of implementation of the ERAS (enhanced recovery after surgery) protocol in our institute and its impact on hospital length of stay and outcome of surgery.

Enrollment

50 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≤ 60 years,
  • Good nutrition,
  • No systemic infection and
  • Elective laparoscopic surgery

Exclusion criteria

  • Age >75 years,
  • Malnutrition or an organ system infection
  • Associated with obstruction, bleeding, emergency surgery or other surgical intervention
  • Tumor with extensive metastasis
  • Prior to surgery, patient was fasting, underwent gastrointestinal decompression and received nutritional support
  • Previous history of abdominal surgery
  • Patient have previously undergone gastrostomy

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

50 participants in 2 patient groups, including a placebo group

thefast track (FTS group)
Active Comparator group
Treatment:
Procedure: enhanced recovery after surgery program in colorectal cancer surgery
Thecontrolgroup
Placebo Comparator group
Treatment:
Procedure: enhanced recovery after surgery program in colorectal cancer surgery

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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