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Compression Anastomosis Using the Compression Anastomosis Ring (CAR™ 27)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00880984
First Posted: April 14, 2009
Last Update Posted: January 7, 2010
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
novoGI
Information provided by:
Aristotle University Of Thessaloniki
  Purpose

Purpose:

Evaluation of the CAR™ 27 for the creation of compression anastomoses.

Indication:

Compression Anastomosis Ring (CAR™ 27) device for creation of circular anastomoses during colonic or colorectal resection.

Study Design:

Prospective, open labeled study.

Patient Population:

Male or female subjects 18 years of age or older who are scheduled for non emergency laparoscopic or open colonic or colorectal resections. A temporary loop ileostomy/colostomy can be preformed up to the discretion of the surgeon.

No. of Subjects:

15 patients estimated up to three months to enroll.

Duration of Treatment:

During the operation - creation of the anastomosis.

Duration of Follow-up:

Follow-up evaluation will be performed daily while hospitalized, during a post-op clinic visit at approximately 1 month (30 days ± 5 days) including a proctoscopic exam and by phone after 3 months.

Endpoints:

To evaluate the creation of a safe and functioning anastomosis and the occurrence of adverse events related to the use of the CAR™ 27 device.


Condition Intervention
Colorectal Surgery Device: Compression Anastomosis Ring: CAR™ 27

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Compression Anastomosis Using the CAR™ 27

Further study details as provided by Aristotle University Of Thessaloniki:

Primary Outcome Measures:
  • Complications during and post procedure including leaks, bleeding, strictures, device failure, re admission, re operation, extra colonic complications etc [ Time Frame: 3-months ]

Estimated Enrollment: 15
Study Start Date: June 2008
Primary Completion Date: September 2009 (Final data collection date for primary outcome measure)
Intervention Details:
    Device: Compression Anastomosis Ring: CAR™ 27
    Creation of anastomosis in colorectal surgeries using CAR™ 27
    Other Name: CAR™ 27
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Patient is over 18 years old.
  2. Patient is scheduled for a non-emergency procedure.
  3. Subject signs and dates a written informed consent form (ICF) and indicates an understanding of the study procedures.

Exclusion Criteria:

  1. Patient has an allergy to nickel.
  2. Patient has a diagnosis of bowel obstruction, bowel strangulation, peritonitis, bowel perforation, local or systemic infection, ischemic bowel, carcinomatosis or extensively spread inflammatory bowel disease.
  3. Patient is participating in another clinical trial which may affect this study's outcomes.
  4. Patient has been taking regular steroid medication.
  5. Patient has contraindications to general anesthesia.
  6. Patient has preexisting sphincter problems or evidence of extensive local disease in the pelvis.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00880984


Locations
Greece
AHEPA University Hospital of Thessaloniki
Thessaloniki, Greece, 54636
Sponsors and Collaborators
Aristotle University Of Thessaloniki
novoGI
Investigators
Principal Investigator: Spiros Papavramidis, Prof. AHEPA University Hospital of Thessaloniki
  More Information

Responsible Party: Prof. Spyros Papavramidis, AHEPA university Hospital of Thessaloniki
ClinicalTrials.gov Identifier: NCT00880984     History of Changes
Other Study ID Numbers: 08-CAR-07-Gr-01
First Submitted: April 13, 2009
First Posted: April 14, 2009
Last Update Posted: January 7, 2010
Last Verified: July 2009

Keywords provided by Aristotle University Of Thessaloniki:
Colon Anastomosis
Rectum Anastomosis
Intestine
Colorectal Surgery
Colorectal Anastomosis