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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04013347
Other study ID # 08/17 OSS ComEt CBM
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2005
Est. completion date March 21, 2017

Study information

Verified date July 2019
Source Campus Bio-Medico University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Neoadjuvant radio-chemotherapy (NRCT) represents a milestone in the treatment of selected rectal tumours. Ideal time interval between the end of NRCT and surgery is still debated; a 6-8 weeks time interval is considered optimal, but shorter or longer intervals have been associated with better oncological outcomes. Moreover, there is a lack of data about clinical postoperative outcomes and different time intervals after the end of NRCT. Here, effect that different time intervals have on postoperative complications with particular regard to the anastomotic dehiscence have been evaluated.

Methods One hundred-sixty-seven patients underwent surgery after long-course NRCT. Three different time intervals were considered: (0-42; 43-56; >57 days).


Description:

Neoadjuvant radio-chemotherapy (NRCT) represents a milestone in the treatment of selected rectal adenocarcinoma. Even though a 6-8 weeks' time interval after the end of NRCT and surgery is considered ideal, the optimal time for surgery is still controversial.


Recruitment information / eligibility

Status Completed
Enrollment 167
Est. completion date March 21, 2017
Est. primary completion date March 1, 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- patients with rectal adenocarcinoma who underwent to resection after combined NRCT at University Campus Bio-Medico di Roma from January 2005 to March 2015.

To evaluate the anastomotic dehiscence were excluded patients undergone to Abdomino-perineal resection (APR) and 4 patients for whom data were not available.

Study Design


Intervention

Procedure:
Rectal Resection
Low Anterior Resection and Abdominoperineal Resection

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Campus Bio-Medico University

Outcome

Type Measure Description Time frame Safety issue
Primary number of patient with low tumor regression grade rate of low tumor regression grade (1-2) 1 week after surgery
Primary number of patient with surgical complications rate of surgical complications 1 month after surgery
Secondary number of patient with anastomotic dehiscence rate of anastomotic dehiscence 1 month after surgery
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