Prospective Randomized Controlled Study for the Effect of Intravenous Lidocaine on the Tolerability of Early Oral Feeding After Laparoscopic Colorectal Surgery in Patients With Colorectal Cancer
18 Years
N/A
Both
Colorectal Cancer
Trial Information
Prospective Randomized Controlled Study for the Effect of Intravenous Lidocaine on the Tolerability of Early Oral Feeding After Laparoscopic Colorectal Surgery in Patients With Colorectal Cancer
Inclusion Criteria:
- Elective laparoscopic colorectal surgery for colorectal cancer.
- Age > 18 years.
- Informed consent.
Exclusion Criteria:
- Allergy to local anesthetics.
- Severe cardiovascular, hepatic, or renal diseases.
- Pregnant or lactating patients.
- Emergency surgery.
- American Society of Anesthesiologists (ASA) class IV
Type of Study:
Interventional
Study Design:
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Supportive Care
Outcome Measure:
Prevalence of postoperative nausea and vomiting.
Outcome Description:
Intolerance to early postoperative oral feeding is defined as the patient's having either nausea or vomiting, requiring that the patient be non-per oral status.
Outcome Time Frame:
From day of surgery to sixth postoperative day.
Safety Issue:
No
Principal Investigator
Hyung Ook Kim, M.D
Investigator Role:
Principal Investigator
Investigator Affiliation:
Kangbuk Samsung Hospital
Authority:
Korea: Food and Drug Administration
Study ID:
KHO10-1
NCT ID:
NCT01346917
Start Date:
April 2011
Completion Date:
June 2012
Related Keywords:
- Colorectal Cancer
- Colorectal cancer
- Laparoscopic surgery
- Postoperative ileus
- Lidocaine
- Early oral feeding
- Colorectal Neoplasms
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