Colon Cancer Clinical Trial
Single Incision Laparoscopic Surgery in Treating Patients With Colorectal Disease
Summary
This study is being done to evaluate single incision laparoscopic surgery (SILS) for colorectal diseases, compared to multi-port laparoscopic surgery. This study is also intended to standardize the SILS technique for colorectal diseases
Full Description
PRIMARY OBJECTIVES:
I. To report the experience of SILS procedure in the treatment of colorectal disease.
II. To standardize the SILS technique.
OUTLINE:
Patients undergo single incision laparoscopic surgery with GelPort® attachment.
After completion of study treatment, patients are followed up at 2 weeks, 3 and 6 months, and at 1 year.
Eligibility Criteria
Inclusion Criteria:
Patients who are willing to give consent and comply with the evaluation and the treatment schedule
Patients with disease processes limited to the right colon; this will include Crohn's disease, polyp disease, and cancers of the right colon
American Society of Anesthesiologists (ASA) =< 3
Exclusion Criteria:
Inability to obtain informed consent
Previous right colon surgery
Previous extensive abdominal surgery that would limit the laparoscopic approach
Stage IV disease at surgery
Metastatic disease diagnosed by computed tomography (CT), magnetic resonance imaging (MRI), or nuclear imaging
Patient enrolled in other interventional study
ASA score greater than 3
Any condition which precludes compliance with the study (Investigator discretion)
Co-morbid condition(s) that could limit the subject's ability to participate in the study or to comply with follow-up requirements, or that could impact the scientific integrity of the trial
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There is 1 Location for this study
Columbus Ohio, 43210, United States
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