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Bilioenteric Anastomosis by Magnetic Compressive Technique

Bilioenteric Anastomosis by Magnetic Compressive Technique: A Prospective, Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03774589
Acronym
BAMCT
Enrollment
200
Registered
2018-12-13
Start date
2019-02-01
Completion date
2022-01-31
Last updated
2019-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bile Duct Injury, Biliary Calculi, Cholangiocarcinoma, Choledochal Cyst, Pancreatic Cancer

Keywords

bilioenteric anastomosis, magnetic compressive technique, morbidity

Brief summary

The purpose of this study is to determine whether the magnetic compressive anastomosis has a better outcomes than traditional manual anastomosis on bilioenteric anastomosis.

Detailed description

The bilioenteric anastomosis is one of the most common and difficult operations in Hepatobiliary Surgery. The traditional manual anastomosis has become one of the main prognosis factors because of the length of suture time, the difficulty of operation, the high incidence of anastomotic leakage and stricture. Magnetic compressive anastomosis can realize the fast anastomosis, reduce the difficulty, and reduce the incidence of anastomotic leakage and stricture. Currently, the majority of studies of magnetic compressive bilioenteric anastomosis are merely confined within clinical case report and single-center, small sample, retrospective study. This study is a prospective, randomized controlled trial. To evaluate the security, reliability and convince of magnetic compressive bilioenteric anastomosis versus traditional suture method on incidence of anastomotic leakage and stricture between magnetic compressive anastomosis and traditional manual anastomosis among patients who need bilioenteric anastomosis operation. The study is to enroll about 200 patients and divide into Study Group (Group A: Magnetic compressive anastomosis) and Control Group (Group B: traditional manual anastomosis) as 1:1 ratio randomly by stratification factors. The incidence of anastomotic leakage and stricture, length of bilioenteric anastomosis time, value of serum bilirubin, length of discharge time of magnetic device and mean time of hospital stay will be evaluated. The patients will drop out of the study if adverse events happen, active request for dropping out, new-onset severe disease or death. The primary and secondary end point will be observed by regular follow-up.

Interventions

The magnetic compressive anastomosis will be used to complete the anastomosis during bilioenteric anastomosis.

A handsewn technique will be used to complete the anastomosis during bilioenteric anastomosis.

Sponsors

Xi'an Jiaotong University
CollaboratorOTHER
Northwest Institute for Non-ferrous Metal Research
CollaboratorUNKNOWN
First Affiliated Hospital Xi'an Jiaotong University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Patients with age between 18 to 75 * Patients' gender was not limited * Patients who were well-diagnosed and had the indication for bilioenteric anastomosis. * Patients whose lifetimes will be longer than 12 months. * Patients who are willing to join this clinical trial and informed consent form voluntarily.

Exclusion criteria

* Woman during pregnancy or lactation or anyone with mental disorder * The wall of hepatic duct or jejunum was too thick so that the attractive force of magnetic device cannot meet the requirements of compression. * Any anatomical variation in bile ducts system or the inner diameter is too small so that the magnetic device cannot place in. * Any foreign body has been implanted in body, such as heart pacemaker. * Surgical contraindication, including: Child-Pugh C with hepatic encephalopathy Anyone with heart, lung, kidney dysfunction or other organ dysfunction, and cannot tolerate surgery.Hepatic ducts stone disease, who was diagnosed as Acute Cholangitis of Severe Type, especially complicated with bacteremia or septic shock. End stage disease, complicated with biliary cirrhosis or portal hypertension.Patients with long- term obstructive jaundice, dehydration, electrolyte disturbance or coagulation defects; Patients have the tendency or history of bleeding. • Any other disease in perioperation periods which needs MRI examination in the next 8 weeks post operation.

Design outcomes

Primary

MeasureTime frameDescription
Bilioenteric anastomotic leakage1 month post operationTo compare the incidence of biliary leakage after magnetic or hand-sewn anastomosis

Secondary

MeasureTime frameDescription
Length of bilioenteric anastomosis timeduring operationTo compare the anastomotic time between magnetic and hand-sewn groups
Time from the date of operation to expel of the magnets.1 to 4 weeks postoperationTo confirm the safe discharge of the magnets
average length of postoperative hospital stay3 monthsTo compare the length of stay between magnetic and hand-sewn groups
Bilioenteric anastomotic stricture1,3,6,12-month post operationTo compare the long-term outcome between magnetic and hand-sewn groups

Countries

China

Contacts

Primary ContactYi Lv, MD,PHD
luyi169@126.com86-29-85323900
Backup ContactXu-Feng Zhang, MD, PhD
xfzhang125@126.com86-29-85323626

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026