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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01453556
Other study ID # Intraextra01
Secondary ID
Status Recruiting
Phase N/A
First received October 13, 2011
Last updated October 20, 2011
Start date October 2011
Est. completion date September 2014

Study information

Verified date October 2011
Source Scientific Institute San Raffaele
Contact Andrea Vignali, MD
Phone 0339 02 2643 2272
Email maxbisso@gmail.com
Is FDA regulated No
Health authority Italy: Ministry of HealthItaly: National Bioethics CommitteeItaly: National Institute of HealthItaly: National Monitoring Centre for Clinical Trials - Ministry of Health
Study type Interventional

Clinical Trial Summary

Verify with a prospective randomised trial if intracorporeal mechanical anastomosis in laparoscopic right colectomy reduces post-operative bowel canalisation time and length of stay in comparison with extracorporeal mechanical anastomosis.


Recruitment information / eligibility

Status Recruiting
Enrollment 158
Est. completion date September 2014
Est. primary completion date September 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age 18 or more

- Benign o neoplastic disease of right colon

- Elective laparoscopic surgery

Exclusion Criteria:

- Emergency surgery

- Adhesion or infiltration of near organs

- Severe heart disease ( New York Heart Association class > 3 )

- Severe respiratory disease ( arterial PO2 < 70 torr )

- Severe Liver disease (Child-Pugh class C)

- Ongoing infections

- Number of plasmatic neutrophil < a 2.0 x 10 9/L

- Other contraindications to laparoscopy

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Laparoscopic right colectomy
Laparoscopic right colectomy with mechanical ileo-colon anastomosis L-L

Locations

Country Name City State
Italy San Raffaele Scientific Institute Milan MI

Sponsors (1)

Lead Sponsor Collaborator
Scientific Institute San Raffaele

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Post-operative canalisation time and length of stay Comparison of post-operative bowel movement time (fist flastus and first dejection) and overall length of stay between the two study groups Post-operative stay (about 7 days) No
Secondary Impact of post-operative ileum and complications. Valuation of global costs Comparison of post-operative short and long-term complications (in particular post-operative ileum) between the two study groups. Valuation of global costs differences. 12 months Yes
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