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Diverting Stoma and Postoperative Morbidity After Low Anterior Resection for Rectal Cancer Within an Enhanced Recovery After Surgery,ERAS, Program


N/A
18 Years
90 Years
Open (Enrolling)
Both
Loopileostomy, Fast Track Program,(Enhanced Recovery After Surgery (ERAS))

Thank you

Trial Information

Diverting Stoma and Postoperative Morbidity After Low Anterior Resection for Rectal Cancer Within an Enhanced Recovery After Surgery,ERAS, Program


See above.


Inclusion Criteria:



- all patients operated with low anterior resection for rectal cancer at Ersta Hospital
between 2002 and 2011 registrated in ERAS database

Exclusion Criteria:

- none

Type of Study:

Observational

Study Design:

Observational Model: Cohort, Time Perspective: Retrospective

Outcome Measure:

Clinical anastomotic leakage

Outcome Description:

Evaluate if a diverting stoma after low anterior resection affects postoperative Morbidity in patients treaated within an ERAS program

Outcome Time Frame:

0 to 9 years after surgery

Safety Issue:

Yes

Principal Investigator

Kajsa Anderin, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Karolinska Institutet

Authority:

Sweden: The National Board of Health and Welfare

Study ID:

2012/538-31/1

NCT ID:

NCT01789515

Start Date:

May 2012

Completion Date:

December 2013

Related Keywords:

  • Loopileostomy
  • Fast Track Program,(Enhanced Recovery After Surgery (ERAS))

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