Uhmontpellier
Montpellier, 34295, France
NCT Number: NCT04495023
Aim of the study :
To evaluate postoperative outcomes of elective left-sided colectomy in a renal transplanted population.
Methods :
From 2010 to 2015, all consecutive patients who underwent left elective colectomy in a referral center were prospectively collected.
Considering our exclusion criterial, data from 120 patients were analyzed. The cohort was separated into 2 groups : renal transplanted patients (KTR-group) and non-renal transplanted patients (C-group) Short and longterm outcomes were compared between the two groups.
Primary outcome :
90 days postoperative anastomotic leak rate
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Notify Me18 year–99 year
All sexes
Observational
Montpellier, 34295, France
From January 2010 to December 2015, data from patients requiring an elective left colectomy for benign or malignant indication were collected prospectively in our colorectal surgery database.
According to our exclusion criterial patients were retrospectively divided into two groups: kidney transplant recipients (KTR-group) and control group (C-group).
The surgical indication for an oncologic left colectomy was retained by the expert surgeon, after a multidisciplinary conversation meeting comprising at least one surgeon, one gastroenterologist, one nephrologist, one radiologist and one oncologist. The surgical indication for diverticular disease was based on French guidelines.
Demographic, clinical, intraoperative and postoperative, histological, length of hospital stay and mortality data were collected over a 90-day period following the intervention.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Open or laparoscopic left elective colectomy with colo-rectal anastomosis
Time frame: 90 days postoperative
Anastomotic leak according to the International Study Group of Rectal Cancer
Time frame: 1 day
Status at the date of latest news
University Hospital, Montpellier
Other
Left Elective Colectomy in Renal Transplanted Patients : a Case-control Study (LECoRT Study)
Acronym: LECoRT
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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