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NCT03928678 Clinical Trial

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

Cancer of Colon Clinical Trial

Official title:
Enhanced Recovery After Surgery Program (ERAS) in Colorectal Cancer Surgery

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03928678
Other study ID # 458
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 1, 2019
Est. completion date December 1, 2020

Study information
Verified date April 2020
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Completed
Enrollment 50
Est. completion date December 1, 2020
Est. primary completion date November 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• enhanced recovery after surgery program in colorectal cancer surgery
to determine the feasibility of implementation of the ERAS protocol in our institute and its impact on hospital length of stay and outcome of surgery.

Locations
Country Name City State
Egypt South Egypt Cancer Instuite Assuit

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary length of hospital stay in days length of hospital stay in days 4 days
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