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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00635466
Other study ID # Lap RC
Secondary ID NCCHCT19-49
Status Active, not recruiting
Phase Phase 2
First received March 6, 2008
Last updated June 15, 2011
Start date February 2008
Est. completion date September 2015

Study information

Verified date June 2011
Source Japan Society of Laparoscopic Colorectal Surgery
Contact n/a
Is FDA regulated No
Health authority Japan: Japan Clinical Oncology Group
Study type Interventional

Clinical Trial Summary

The purpose of this study is to examine the technical and oncological feasibility of laparoscopic surgery for rectal carcinoma


Description:

Recently reported randomized controlled trials demonstrated that laparoscopic surgery was comparable or superior to open surgery regarding the long-term outcome for colon and rectosigmoidal carcinoma; however, controversy persists regarding the appropriateness of laparoscopic surgery for patients with rectal carcinoma because of the uncertainty of the long-term outcome, and of concerns over the safety of the procedure. In Japan, lateral lymph node dissection combined with total mesorectal excision remains the standard surgical procedure for patients with advanced lower rectal carcinoma, and lateral lymph node dissection by laparoscopy is still an unexplored frontier. To examine the technical and oncological feasibility of laparoscopic surgery for rectal carcinoma, a phase II trial will be conducted in patients with a preoperative diagnosis of stage 0/I rectal carcinoma, under the direction of the Japan Society of Laparoscopic Colorectal Surgery, to which leading hospitals in laparoscopic surgery for colorectal carcinoma in Japan are members.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 495
Est. completion date September 2015
Est. primary completion date September 2015
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 75 Years
Eligibility Inclusion Criteria:

1. Histologically proven rectal carcinoma.

2. Tumor located in the rectum.

3. Clinical Tis, T1, T2 N0 M0

4. Without multiple lesions other than carcinoma in situ

5. Tumor size <8 cm.

6. Sufficient organ function.

7. No bowel obstruction.

8. No history of major colorectal surgery.

9. No history of chemotherapy or radiotherapy.

10. Provide written informed consent.

Exclusion Criteria:

1. Synchronous or metachronous (within 5 years) malignancy other than carcinoma in situ.

2. Pregnant or lactating women.

3. Severe mental disease.

4. Severe pulmonary emphysema, interstitial pneumonitis or ischemic heart disease.

5. Continuous systemic steroid therapy.

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
laparoscopic surgery for rectal carcinoma
Laparoscopic resection of the rectum with adequate lymphadenectomy is performed according to the General Rules for Clinical and Pathological Studies on Cancer of the Colon, Rectum and Anus edited by the Japanese Society for Cancer of the Colon and Rectum. The extent of lymphadenectomy and site of ligation and division of the inferior mesenteric vessels were decided by the surgeon in charge. Pneumoperitoneal approaches are used to explore the abdomen, mobilize the left side colon, identify critical structures and ligate the vascular pedicle. Mobilization of the rectum, excision of the mesorectum, rectal transection, removal of the specimen, and reconstruction are performed by the pneumoperitoneal approach or the extracorporeal approach via a small incision (<8 cm).

Locations

Country Name City State
Japan Kitasato University Hospital Sagamihara Kanagawa

Sponsors (1)

Lead Sponsor Collaborator
Japan Society of Laparoscopic Colorectal Surgery

Country where clinical trial is conducted

Japan, 

References & Publications (1)

Yamamoto S, Yoshimura K, Konishi F, Watanabe M. Phase II trial to evaluate laparoscopic surgery for Stage 0/I rectal carcinoma. Jpn J Clin Oncol. 2008 Jul;38(7):497-500. doi: 10.1093/jjco/hyn054. Epub 2008 Jun 26. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary overall survival 5 year Yes
Secondary anastomotic leakage rate 1 month Yes
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