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REinforcement of the Pancreas in distaL pAncreatectomY (REPLAY)

Does the Strengthening of the Pancreas in Distal Pancreatectomy Using Endo GIA Reload Reinforced Reduce the Occurrence of Pancreatic Fistula? Multicenter Randomized Prospective Open Study

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03030170
Acronym
REPLAY
Enrollment
207
Registered
2017-01-24
Start date
2017-06-28
Completion date
2021-07-30
Last updated
2023-08-09

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

Conditions

Distal Pancreatectomy (DP)

Brief summary

Despite an improvement regarding morbidity and mortality since 30 years, especially in expert centers, pancreatic surgery remains currently associated to a significant postoperative morbidity reaching more than 60%. Regarding distal pancreatectomy (DP), the main complication following surgery is the occurrence of postoperative pancreatic fistula (PF) which may be able to lead an increased risk of bleeding, gastroparesis and finally a longer hospital stays. The main risk factors associated to the occurrence of pancreatic fistula are represented by the texture of the pancreatic parenchyma (soft pancreas) and the caliber of the main pancreatic duct (\<3mm). Looking for new means of reducing the occurrence of pancreatic fistula is a priority in pancreatic surgery and a genuine public health issue. Currently, no formal recommendations concerning the optimal technical for closure of the distal stump in DP are available. In fact, manual closing by elective suturing or stapling of the main pancreatic duct give similar results. The use of a reinforcing stapling potentially represents a simple way to decrease the occurrence of pancreatic fistula and requires evaluation by a prospective randomized study.

Interventions

DEVICEENDO GIA X-tra Thick reload with Tri Staple Technology

Suture of the pancreas by normal stapling

DEVICEENDO GIA Articulating Reinforced Reload with Tri-Staple Technology

Suture of the pancreas by reinforced stapling

Sponsors

Rennes University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

intervention with reinforced medical device, or not

Eligibility

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

Inclusion criteria

* All patients who undergo DP whether made by open or laparoscopic surgery * Patients 18 years of age or older, * Benefiting from a social security scheme, * Having given his free, informed and written consent.

Exclusion criteria

* History of pancreatic abdominal surgery * Severe co-morbidity type renal failure requiring hemodialysis, unbalanced diabetes, major respiratory insufficiency, heart failure ≥ stage 3 NYHA; * Persons of full age who are subject to legal protection, persons deprived of liberty. * Pregnant or nursing women * Patients participating in or participating in another study

Design outcomes

Primary

MeasureTime frame
Rate of postoperative pancreatic fistula defined by the criteria of the ISGPFup to 90 days

Secondary

MeasureTime frame
Gravity of the pancreatic fistula according to the 3 stages of ISGPFup to 90 days
Assessment of the occurrence of gastroparesis and its severity according to the criteria of ISGPSup to 90 days
Evaluation of the occurrence of postoperative haemorrhageup to 90 days
Perioperative mortality and 90-day mortalityup to 90 days
Overall morbidity classified and categorized according to the classification of Dindo and Clavienuntil 90 days
Rehospitalization ratesuntil 90 days
Length of hospital stayup to 90 days

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026