Abdominal Drainage vs Postoperative Antibiotico-prophylaxis vs Control in Laparoscopic Right Hemicolectomy With Intracorporeal Anastomosis for Right Colon Cancer
Primary Purpose
Colon Cancer
Status
Unknown status
Phase
Early Phase 1
Locations
Study Type
Interventional
Intervention
abdominal drainage
Postoperative antibiotico-prophylaxis
Sponsored by
About this trial
This is an interventional treatment trial for Colon Cancer focused on measuring intracorporeal anastomosis, right hemicoletomy, colon cancer
Eligibility Criteria
Inclusion Criteria:
- Right colon cancer
- Intracorporeal anastomosis
- Laparoscopic surgery
- Elective surgery
- informed consent signed
Exclusion Criteria:
- below 18 years old
- IBD
- ASA IV
- T4b
- Metastatic disease
- Preoperative steroids
- Conversion to open surgery
- Emergency surgery
- concomitant major operation
- preoperative infective status
- benign disease
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
No Intervention
Arm Label
Abdominal drainage
Postoperative antibiotico-prophylaxis
Control group
Arm Description
19 Fr abdominal drainage placed intraoperatevely in right paracolic gutter
postoperative antibiotico-prophylaxis with Ceftriaxone 2gr and Metronidazole 1.5gr
No drainage nor postoperative antibiotico-prophylaxis
Outcomes
Primary Outcome Measures
C-Reactive Proteine
measured mg/L in I and III POD
Secondary Outcome Measures
White blood cell
measured thousands/mL in I and III POD
Procalcitonine
measured ng/ml in III and V POD
Days of hospitalization
number of days of hospitalization
Readmission rate
rate of hospital readmission
Mortality rate
postoperative mortality
Surgical site infection rate
postoperative wound infection
Anastomotic leak rate
postoperative Ileocolic anastomotic leakage
Tolerance to liquid diet
time to clear fluid tolerance
Tolerance to solid diet
time to light diet tolerance
Time to first flatus
Time to first flatus postoperatively
Time to first evacuation
Time to first evacuation postoperatively
need of abdomen CTscan rate
need of abdomen CTscan
Full Information
NCT ID
NCT04977882
First Posted
July 15, 2021
Last Updated
July 25, 2021
Sponsor
University of Rome Tor Vergata
1. Study Identification
Unique Protocol Identification Number
NCT04977882
Brief Title
Abdominal Drainage vs Postoperative Antibiotico-prophylaxis vs Control in Laparoscopic Right Hemicolectomy With Intracorporeal Anastomosis for Right Colon Cancer
Official Title
Abdominal Drainage vs Postoperative Antibiotico-prophylaxis vs Control in Laparoscopic Right Hemicolectomy With Intracorporeal Anastomosis for Right Colon Cancer.
Study Type
Interventional
2. Study Status
Record Verification Date
July 2021
Overall Recruitment Status
Unknown status
Study Start Date
September 1, 2021 (Anticipated)
Primary Completion Date
November 1, 2022 (Anticipated)
Study Completion Date
January 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Rome Tor Vergata
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Monocentric pilot prospective randomized study with 3 cohorts: abdominal drainage vs postoperative antibioticoprophylaxis vs none in patients undergoing laparoscopic right hemicolectomy with introcorporeal anastomosis for right colon cancer
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colon Cancer
Keywords
intracorporeal anastomosis, right hemicoletomy, colon cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
75 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Abdominal drainage
Arm Type
Experimental
Arm Description
19 Fr abdominal drainage placed intraoperatevely in right paracolic gutter
Arm Title
Postoperative antibiotico-prophylaxis
Arm Type
Experimental
Arm Description
postoperative antibiotico-prophylaxis with Ceftriaxone 2gr and Metronidazole 1.5gr
Arm Title
Control group
Arm Type
No Intervention
Arm Description
No drainage nor postoperative antibiotico-prophylaxis
Intervention Type
Procedure
Intervention Name(s)
abdominal drainage
Intervention Description
19 Fr abdominal drainage placed intraoperatively in right colic gutter
Intervention Type
Drug
Intervention Name(s)
Postoperative antibiotico-prophylaxis
Intervention Description
Ceftriaxone 2 gr and Metronidazole 1.5 gr per day for 2 days postoperatively
Primary Outcome Measure Information:
Title
C-Reactive Proteine
Description
measured mg/L in I and III POD
Time Frame
30 days postoperatively
Secondary Outcome Measure Information:
Title
White blood cell
Description
measured thousands/mL in I and III POD
Time Frame
30 days postoperatively
Title
Procalcitonine
Description
measured ng/ml in III and V POD
Time Frame
30 days postoperatively
Title
Days of hospitalization
Description
number of days of hospitalization
Time Frame
90 days postoperatively
Title
Readmission rate
Description
rate of hospital readmission
Time Frame
90 days postoperatively
Title
Mortality rate
Description
postoperative mortality
Time Frame
90 days postoperatively
Title
Surgical site infection rate
Description
postoperative wound infection
Time Frame
30 days postoperatively
Title
Anastomotic leak rate
Description
postoperative Ileocolic anastomotic leakage
Time Frame
30 days postoperatively
Title
Tolerance to liquid diet
Description
time to clear fluid tolerance
Time Frame
30 days postoperatively
Title
Tolerance to solid diet
Description
time to light diet tolerance
Time Frame
30 days postoperatively
Title
Time to first flatus
Description
Time to first flatus postoperatively
Time Frame
30 days postoperatively
Title
Time to first evacuation
Description
Time to first evacuation postoperatively
Time Frame
30 days postoperatively
Title
need of abdomen CTscan rate
Description
need of abdomen CTscan
Time Frame
30 days postoperatively
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Right colon cancer
Intracorporeal anastomosis
Laparoscopic surgery
Elective surgery
informed consent signed
Exclusion Criteria:
below 18 years old
IBD
ASA IV
T4b
Metastatic disease
Preoperative steroids
Conversion to open surgery
Emergency surgery
concomitant major operation
preoperative infective status
benign disease
12. IPD Sharing Statement
Learn more about this trial
Abdominal Drainage vs Postoperative Antibiotico-prophylaxis vs Control in Laparoscopic Right Hemicolectomy With Intracorporeal Anastomosis for Right Colon Cancer
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