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The Effectiveness of Adding Braun Anastomosis to Standard Child Reconstruction After Pancreatoduodenectomy (REMBRANDT)

Primary Purpose

Pancreatic Disease, Pancreatic Cancer, Delayed Gastric Emptying

Status
Recruiting
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Braun anastomosis
Standard Child reconstruction
Sponsored by
Radboud University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pancreatic Disease focused on measuring Randomized controlled trial, Prospective studies, Braun anastomosis, Braun enteroenterostomy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Undergoing open pancreatoduodenectomy Provided informed consent Age over 18 years Exclusion Criteria: Insufficient control of the Dutch language to read the patient information and to fill out the questionnaires in Dutch hospitals Previous bariatric surgery (such as Roux-en-Y gastric bypass, gastric sleeve) Pregnancy Bowel motility disorders Minimally invasive pancreatoduodenectomy

Sites / Locations

  • Amsterdam UMC
  • OLVG
  • Catharina hospital
  • Medical spectrum Twente
  • Groningen UMC
  • Medical center Leeuwarden
  • LUMC
  • Maastricht UMC+
  • St Antonius hospital
  • Radboud UMCRecruiting
  • Erasmus MC
  • Isala hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Braun anastomosis

Standard Child reconstruction

Arm Description

Open pancreatoduodenectomy with Braun enteroenterostomy

Open pancreatoduodenectomy only

Outcomes

Primary Outcome Measures

Delayed gastric emptying (DGE)
DGE is defined by the need for maintenance of the nasogastric tube (NGT), need for reinsertion of NGT for persistent vomiting after postoperative day (POD) 7, or inability to tolerate a solid diet.

Secondary Outcome Measures

Pancreatic fistula (POPF)
Any measurable volume of drain output with an amylase level of more than 3 times the upper limit of normal serum amylase and clinically relevant condition or development of the patient directly related to the POPF.
Anastomotic leak
Anastomotic leaks of the hepatojejunostomy (HJ) or Braun enteroenterostomy (BE). Anastomotic leaks of the HJ manifest as bile leakage. This is defined as "fluid with an increased bilirubin concentration in the abdominal drain or in the intra-abdominal fluid on or after postoperative day 3, or as the need for radiologic intervention because of biliary collections or relaparotomy resulting from bile peritonitis. Increased bilirubin in the drain is defined as bilirubin concentration more than 3 times greater than the serum bilirubin concentration. An anastomotic leak of the BE is present when an abdominal CT with contrast shows leakage of contrast from the BE or when during relaparotomy dehiscence of the BE is apparent.
Postoperative complications: incidence and severity
Scored according to the modified Clavien-Dindo classification for surgical complications. Grade III and higher are considered clinically relevant in this study.
Number of days participants were hospitalized
The time period in days between hospital admission and discharge from the hospital.
Number of participants with in-hospital mortality
Any death during hospital admission.
30-day mortality
Any death occurring 30 days after pancreatoduodenectomy.
Quality of life (QoL) based on five dimensions
The EQ-5D-5L standardized questionnaire will be used.
Participants perceived disease and treatment related quality of life
The European Organisation for Research and Treatment of Cancer (EORTC) QLQ-C30/PAN26 standardized quality of life questionnaires will be used.
Quality of recovery
The QoR-15 standardized questionnaire will be used.
Functional outcome at 12 months
Participants will be phoned to assess whether they have complaints of delayed gastric emptying ("afferent loop syndrome").

Full Information

First Posted
January 24, 2023
Last Updated
April 25, 2023
Sponsor
Radboud University Medical Center
Collaborators
Rising Tide Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT05709197
Brief Title
The Effectiveness of Adding Braun Anastomosis to Standard Child Reconstruction After Pancreatoduodenectomy
Acronym
REMBRANDT
Official Title
The Effectiveness of Adding Braun Anastomosis to Standard Child Reconstruction to Reduce Delayed Gastric Emptying After Pancreatoduodenectomy (REMBRANDT): a Multicenter Randomized-controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 17, 2023 (Actual)
Primary Completion Date
September 2025 (Anticipated)
Study Completion Date
September 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Radboud University Medical Center
Collaborators
Rising Tide Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The goal of this clinical trial (REMBRANDT) is to evaluate the effectiveness of adding an extra connection (i.e. 'Braun anastomosis') after standard reconstruction in pancreatic head resection in reducing the incidence of delayed gastric emptying.
Detailed Description
Rationale/hypothesis: The addition of Braun enteroenterostomy (BE) reduces the incidence of delayed gastric emptying (DGE) resulting in lower morbidity and healthcare costs after pancreatoduodenectomy. Objective: To assess the effectiveness of adding BE in reducing DGE in patients undergoing open pancreatoduodenectomy. Study design: A multicenter, patient and observer blinded, registry-based randomized controlled trial. Study population: Patients undergoing an open pancreatoduodenectomy for all indications. Intervention: Braun enteroenterostomy (BE), or Braun anastomosis, in addition to usual care. Usual care/comparison: Pancreatoduodenectomy with standard Child reconstruction. Main endpoints: Incidence of DGE Grade B/C (according to International Study Group of Pancreatic Surgery (ISGPS) Incidence of postoperative pancreatic fistulas (POPF) Grade B/C (according to ISGPS), anastomotic leak, complications, hospital length of stay, functional outcome at 12 months, in-hospital mortality, 30-day mortality, healthcare costs. Sample size: 256 in total, 128 per arm Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Patients undergoing open pancreatoduodenectomy have an increased risk of postoperative complications such as DGE, POPF and anastomotic leak. The addition of BE, which is an anastomosis, could also result in a leak. However, this risk is diminishable compared to the risks of DGE and DGE related other complications like anastomotic leaks associated with standard pancreatoduodenectomy. Moreover, previous cohort studies involving BE do not describe an increased risk of adverse outcomes for BE.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Disease, Pancreatic Cancer, Delayed Gastric Emptying
Keywords
Randomized controlled trial, Prospective studies, Braun anastomosis, Braun enteroenterostomy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Masking Description
Patients will be blinded considering their treatment allocation. The house officer, ward nurses and data managers who extract data concerning the primary and secondary endpoint will be blinded for the allocation as well. For this reason, this will be a patient- and observer blinded RCT.
Allocation
Randomized
Enrollment
256 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Braun anastomosis
Arm Type
Experimental
Arm Description
Open pancreatoduodenectomy with Braun enteroenterostomy
Arm Title
Standard Child reconstruction
Arm Type
Other
Arm Description
Open pancreatoduodenectomy only
Intervention Type
Procedure
Intervention Name(s)
Braun anastomosis
Intervention Description
Participants will undergo open pancreatoduodenectomy (PD). The reconstruction technique will not be standardized. In addition to the reconstruction technique used, a side-to-side anastomosis will be created between the afferent and efferent jejunal limbs of the gastrojejunostomy (GJ) at 20 cm distance from the GJ. The anastomosis will be hand-sewn with monofilament PDS 3-0 one-layer running suture.
Intervention Type
Procedure
Intervention Name(s)
Standard Child reconstruction
Intervention Description
Participants will undergo open pancreatoduodenectomy (PD). The reconstruction technique will not be standardized. The surgeon is able to perform the PD as normally would be done (antecolic, retrocolic, pylorus-preserving or with distal gastric resecting).
Primary Outcome Measure Information:
Title
Delayed gastric emptying (DGE)
Description
DGE is defined by the need for maintenance of the nasogastric tube (NGT), need for reinsertion of NGT for persistent vomiting after postoperative day (POD) 7, or inability to tolerate a solid diet.
Time Frame
During hospitalization
Secondary Outcome Measure Information:
Title
Pancreatic fistula (POPF)
Description
Any measurable volume of drain output with an amylase level of more than 3 times the upper limit of normal serum amylase and clinically relevant condition or development of the patient directly related to the POPF.
Time Frame
During hospitalization
Title
Anastomotic leak
Description
Anastomotic leaks of the hepatojejunostomy (HJ) or Braun enteroenterostomy (BE). Anastomotic leaks of the HJ manifest as bile leakage. This is defined as "fluid with an increased bilirubin concentration in the abdominal drain or in the intra-abdominal fluid on or after postoperative day 3, or as the need for radiologic intervention because of biliary collections or relaparotomy resulting from bile peritonitis. Increased bilirubin in the drain is defined as bilirubin concentration more than 3 times greater than the serum bilirubin concentration. An anastomotic leak of the BE is present when an abdominal CT with contrast shows leakage of contrast from the BE or when during relaparotomy dehiscence of the BE is apparent.
Time Frame
During hospitalization
Title
Postoperative complications: incidence and severity
Description
Scored according to the modified Clavien-Dindo classification for surgical complications. Grade III and higher are considered clinically relevant in this study.
Time Frame
During hospitalization
Title
Number of days participants were hospitalized
Description
The time period in days between hospital admission and discharge from the hospital.
Time Frame
During hospitalization
Title
Number of participants with in-hospital mortality
Description
Any death during hospital admission.
Time Frame
During hospitalization
Title
30-day mortality
Description
Any death occurring 30 days after pancreatoduodenectomy.
Time Frame
30 days
Title
Quality of life (QoL) based on five dimensions
Description
The EQ-5D-5L standardized questionnaire will be used.
Time Frame
Change from baseline at 1 week, at 2 weeks, and 3 months
Title
Participants perceived disease and treatment related quality of life
Description
The European Organisation for Research and Treatment of Cancer (EORTC) QLQ-C30/PAN26 standardized quality of life questionnaires will be used.
Time Frame
Change from baseline at 2 weeks, 3 months, and 12 months
Title
Quality of recovery
Description
The QoR-15 standardized questionnaire will be used.
Time Frame
Change from baseline at 1 week, at 2 weeks, and 3 months
Title
Functional outcome at 12 months
Description
Participants will be phoned to assess whether they have complaints of delayed gastric emptying ("afferent loop syndrome").
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Undergoing open pancreatoduodenectomy Provided informed consent Age over 18 years Exclusion Criteria: Insufficient control of the Dutch language to read the patient information and to fill out the questionnaires in Dutch hospitals Previous bariatric surgery (such as Roux-en-Y gastric bypass, gastric sleeve) Pregnancy Bowel motility disorders Minimally invasive pancreatoduodenectomy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Bo TM Strijbos, MD
Phone
0031243668086
Ext
0031631987808
Email
bo.strijbos@radboudumc.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Martijn WJ Stommel, MD, PhD
Organizational Affiliation
Radboud University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Amsterdam UMC
City
Amsterdam
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
M G Besselink
Facility Name
OLVG
City
Amsterdam
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
M F Gerhards
Facility Name
Catharina hospital
City
Eindhoven
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
I de Hingh
Facility Name
Medical spectrum Twente
City
Enschede
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
M Liem
Facility Name
Groningen UMC
City
Groningen
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
J M Klaase
Facility Name
Medical center Leeuwarden
City
Leeuwarden
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
E R Manusama
Facility Name
LUMC
City
Leiden
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
J SD Mieog
Facility Name
Maastricht UMC+
City
Maastricht
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
M den Dulk
Facility Name
St Antonius hospital
City
Nieuwegein
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
H C van Santvoort
Facility Name
Radboud UMC
City
Nijmegen
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
B TM Strijbos
Facility Name
Erasmus MC
City
Rotterdam
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
B Groot Koerkamp
Facility Name
Isala hospital
City
Zwolle
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
V B Nieuwenhuijs

12. IPD Sharing Statement

Learn more about this trial

The Effectiveness of Adding Braun Anastomosis to Standard Child Reconstruction After Pancreatoduodenectomy

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