Anal Sphincter Prosthesis in Treating Patients Who Are Undergoing Surgery for Anal or Rectal Cancer



Status:Recruiting
Conditions:Colorectal Cancer, Cancer, Cancer, Hospital
Therapuetic Areas:Oncology, Other
Healthy:No
Age Range:Any
Updated:2/4/2013
Start Date:January 2003

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Total Anorectal Reconstruction With The American Medical Systems, Inc. Acticon Neosphincter Prosthesis After Abdominoperineal Resection


RATIONALE: An anal sphincter prosthesis may replace the need for a permanent colostomy and
may improve the quality of life of patients who are undergoing surgery for anal or rectal
cancer.

PURPOSE: Clinical trial to study the effectiveness of an anal sphincter prosthesis in
treating patients who have anal or rectal cancer and are undergoing surgery to remove the
anus and rectum.


OBJECTIVES:

- Determine the risk of complications and feasibility of total anorectal reconstruction
using the Acticon Neosphincter prosthesis after abdominoperineal resection in patients
with anal or rectal cancer.

- Determine continence, bowel function, and quality of life of patients treated with this
surgery.

OUTLINE: Patients undergo abdominoperineal resection (APR) with perineal colostomy and
diverting loop ileostomy. At least 3 months after APR, patients undergo placement of the
Acticon Neosphincter prosthesis. At least 6 weeks after prosthesis placement, the prosthesis
is activated. When the patient demonstrates the ability to operate the prosthesis, the
ileostomy is reversed.

Quality of life is assessed at 6 and 12 months and then annually thereafter.

Patients are followed at 6 and 12 months and then annually thereafter.

PROJECTED ACCRUAL: At least 20 patients will be accrued for this study.

DISEASE CHARACTERISTICS:

- Histologically confirmed distal rectal or anal cancer

- No recurrent or metastatic disease

- Not at high risk for local recurrence

- Not a candidate for sphincter-preserving surgery

PATIENT CHARACTERISTICS:

Age

- 18 and over

Performance status

- Not specified

Life expectancy

- Not specified

Hematopoietic

- Not specified

Hepatic

- Not specified

Renal

- Not specified

Other

- No active pelvic sepsis

- Acceptable risk for surgery and general anesthesia

- Sufficient dexterity and mental capacity to operate the Acticon Neosphincter
prosthesis

PRIOR CONCURRENT THERAPY:

Biologic therapy

- Not specified

Chemotherapy

- Not specified

Endocrine therapy

- Not specified

Radiotherapy

- Not specified

Surgery

- See Disease Characteristics

Other

- Not other concurrent investigational products
We found this trial at
1
site
1275 York Avenue
New York, New York 10065
212-639-2000
Memorial Sloan-Kettering Cancer Center Memorial Sloan-Kettering Cancer Center — the world's oldest and largest private...
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from
New York, NY
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