Magnetic Compressive Anastomosis for Biliojejunostomy and Pancreaticojejunostomy During Whipple's Procedure

Sponsor
First Affiliated Hospital Xi'an Jiaotong University (Other)
Overall Status
Unknown status
CT.gov ID
NCT03792048
Collaborator
(none)
50
2
2
36
25
0.7

Study Details

Study Description

Brief Summary

Magnetic anastomosis has been attempted in biliary and intestinal reconstruction. Based on our initial experience, the investigators have successfully utilized magnetic anastomosis for biliojejunostomy and pancreaticojejunostomy during pancreaticoduodenectomy. The current study was to design a prospective and case-control study with utilization of magnetic compression anastomosis for pancreaticojejunostomy and biliojejunostomy in Whipple's procedure versus traditional hand-sewn technique on the postoperative morbidity, such as biliary/pancreatic fistula, hemorrhage, anastomotic stenosis, etc. In addition, the investigators are seeking to assess the safety and formation of the anastomosis by magnetic technique.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Magnetic Compressive Anastomosis
N/A

Detailed Description

The magnets used in the current study consists of a mother and daughter magnets. An 8-Fr nasogastric tube is tightly fixed with the mother magnet, which will be used for bile or pancreatic drainage before formation of anastomoses. The outside diameter (OD) of the magnets ranges from 5mm to 15mm. In fact, for biliojejunostomy, larger magnets are applied, whereas for pancreaticojejunostomy, smaller magnets are routinely used. This study is a single-center, parallel controlled trial to evaluate the safety and effectiveness of magnetic compression technique for biliojejunostomy and pancreaticojejunostomy, versus traditional hand-sewn techniques on the postoperative morbidity of the patients. And also how to avoid mutual attraction of the two pairs of magnets, formation of bilio-/pancreaticojejunostomy time, discharge rule of the magnets will be all evaluated in the current study.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Magnetic Compressive Anastomosis for Biliojejunostomy and Pancreaticojejunostomy During Whipple's Procedure: a Prospective Case-control Study
Actual Study Start Date :
Feb 1, 2019
Anticipated Primary Completion Date :
Jan 31, 2021
Anticipated Study Completion Date :
Jan 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Magnetic Compressive Anastomosis

A magnetic device will be used during bilioenteric anastomosis and pancreaticojejunostomy

Procedure: Magnetic Compressive Anastomosis
A magnetic device will be used during bilioenteric anastomosis and pancreaticojejunostomy

No Intervention: Manual Anastomosis

Manual Anastomosis for bilioenteric anastomosis and pancreaticojejunostomy

Outcome Measures

Primary Outcome Measures

  1. Incidence of anastomotic fistula [1 month post operation]

    Incidence of biliary or pancreatic fistula after surgery

Secondary Outcome Measures

  1. Length of bilio-/pancreaticojejunostomy time [during operation]

    Separate operation time of magnetic anastomosis for bilio- and pancreaticojejunostomy

  2. average length of postoperative hospital stay [1 to 4 weeks postoperation]

    length of hospital stay (days) after surgery

  3. Hospitalization cost [1 to 4 weeks postoperation]

    cost in hospital

  4. incidence of biliojejunostomic stricture [12 months post operation]

    Incidence of biliojejunostomic stricture between magnetic and manual groups during the relatively long-term follow-up

  5. Incidence of pancreaticojejunostomic stricture [12 months post operation]

    Incidence of pancreaticojejunostomic stricture between magnetic and manual groups during the relatively long-term follow-up

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts 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 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 biliary 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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 First Affiliated Hospital of Xian JiaotongUniversity Xi'an Shaanxi China 710061
2 The First Affiliated Hospital of Xi'an Jiaotong University Xi'an Shaanxi China 710061

Sponsors and Collaborators

  • First Affiliated Hospital Xi'an Jiaotong University

Investigators

  • Principal Investigator: Yi Lv, MD, PhD, First Affiliated Hospital Xi'an Jiaotong University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
First Affiliated Hospital Xi'an Jiaotong University
ClinicalTrials.gov Identifier:
NCT03792048
Other Study ID Numbers:
  • XJTU1AF-CRF-2015-001-2
First Posted:
Jan 3, 2019
Last Update Posted:
Nov 18, 2019
Last Verified:
Nov 1, 2019
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by First Affiliated Hospital Xi'an Jiaotong University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 18, 2019