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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01469442
Other study ID # 08 114 01
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 2009
Est. completion date September 2017

Study information

Verified date July 2020
Source University Hospital, Toulouse
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Aim : Effect of external biliary duct stent after hepatectomy on the occurence of postoperative biliary fistula.

Methods : French prospective multicenter randomized trial. Population study: Adult patients who underwent hepatectomy (> 2 segments) on non-cirrhotic liver.

Hypothesis: decreased postoperative biliary fistula from 15% to 5% with the presence of a external biliary duct stent. With this hypothesis, the number of patients required to be equal to 152 per group for a total of 304 patients.

Outcome measure: Primary : Postoperative biliary complications (biliary fistula, biloma, biliary peritonitis) Secondary : All morbidity, mortality, additional manoeuvres to treat biliary fistula, during of hospital stay and biliary fistula.

Follow up: A follow-up of patients 3 months after surgery for all patients. The planned total duration of the study is 3 years and 3 months.


Description:

After performing the hepatectomy and verification of hemostasis, patients were randomized (external biliary duct stent or not) by sealed envelopes. Systematic intraoperative test with methylene blue or air by the external biliary duct stent (EBDS) will necessary for all patients. Intra-abdominal drainage or not and type will be at the discretion of the surgeon. The EBDS will be left open for the first 7 postoperative days and then clamped. The EBDS will be removed during a consultation 5 weeks after surgery. Both groups of patients will be reviewed at 3 months after surgery, it will be noted at this point the possible complications related to the presence of EBDS (leakage from the drain, drop..). If patients are hospitalized more than five weeks, the study will stop at their consultation three months or the day of the consultation where the DTC is removed if it is still present at 3 months.


Recruitment information / eligibility

Status Completed
Enrollment 304
Est. completion date September 2017
Est. primary completion date September 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Subject has given his informed consent and signed consent

- Hepatectomy at least 2 segments of liver parenchyma for a benign or malignant disease by laparotomy

- Not cirrhotic liver

Exclusion Criteria:

- Surgery made in emergency

- Surgery by laparoscopy

- Need to draw up a bilic-digestive anastomosis

- Liver cirrhosis

- History of cholecystectomy

- Resection of less than 2 segments

- Preoperative jaundice (total bilirubin> 30 micromol / l)

- Presence of preoperative biliary drainage

- Patients requiring the installation of a drain transcystic during the operation

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
External Biliary duct stent in the bile duct by cystic way
The size of the external biliary duct stent depending of cystic duct size

Locations

Country Name City State
France CHU Amiens
France Hotel Dieu Clermont Ferrand
France Hôpital beaujon Clichy
France Hôpital Claude Huriez Lille
France CHU la conception Marseille
France Institut Paoli Calmettes Marseille
France Hôpital St Eloi Montpellier
France Hotel Dieu Nantes
France Hôpital Saint Antoine Paris
France hôpital Haute Pierre Strasbourg
France Toulouse Purpan Toulouse
France Hôpital Paul Brousse Villejuif

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Toulouse

Country where clinical trial is conducted

France, 

References & Publications (1)

Maulat C, Regimbeau JM, Buc E, Boleslawski E, Belghiti J, Hardwigsen J, Vibert E, Delpero JR, Tournay E, Arnaud C, Suc B, Pessaux P, Muscari F. Prevention of biliary fistula after partial hepatectomy by transcystic biliary drainage: randomized clinical tr — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Postoperative biliary fistula 3 forms of diagnosis : bile in the intra-abdominal drainage; presence of an intra-abdominal collection of bile liquid (biloma); presence of an effusion of bile in the abdominal space (biliary peritonitis). 3 months after surgey
Secondary Morbidity additional maneuvers for treat biliary fistula, during of hospital stay, during of biliary fistula 3 months after surgey
Secondary Mortality 3 months after surgery
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