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Completed

NCT Number: NCT03331718

PoLyglycolic Acid Felt reiNforcEmenT of the PancreaticoJejunostomy (PLANET-PJ Trial)

The polyglycolic acid (PGA) felt is a felt-like absorbable suture reinforcing material. The pancreatojejunostomy aimed at reducing POPF is not established at present. We devised a new method using doubly PGA felt. This study is a multicenter, randomized phase III trial between Japan and Korea to verify the usefulness of this double coating of PGA felt.

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Key information

Age range

20 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

University of Toyama

Toyama, 9300194, Japan

About this study

Pancreatojejunostomy is generally a combination of suture between the pancreatic parenchyma and the seromuscular layer of the jejunum, and duct-to-mucosa suture. The clinical study about the various kinds of pancreatojejunostomy have been reported for the purpose of lowering the frequency of POPF; however, the frequency of more than grade B POPF is still around 10 to 20%. In soft pancreas cases with unexpanded pancreatic ducts, the risk is further elevated.

The polyglycolic acid (PGA) felt is an absorbable suture reinforcing material. It is generally used to reinforce sutures of fragile tissues such as the lung, bronchi, liver, and gastrointestinal tract, and to reinforce a wide range of tissue defects. Regarding pancreatojejunostomy using a PGA felt, the incidence of POPF formation was decreased in some retrospective studies; on the other hand, no significant difference was found in other study. As described above, the pancreatojejunostomy aimed at reducing POPF is not established at present. We devised a new method using doubly PGA felt. This study is a multicenter, randomized phase III trial between Japan and Korea to verify the usefulness of this double coating of PGA felt.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Disease of pancreatic or periampullary lesions to require pancreatoduodenectomy
  • Planned pancreaticojejunostomy including duct-to-mucosa anastomosis
  • MPD diameter ≤3mm on the left side of the portal vein in preoperative imaging (CT or MRI)
  • Performance status (ECOG scale): 0-1 at the time of enrollment
  • Age: 20 years or older
  • Adequate organ function A) Leukocyte count: ≥2500 mm3, ≤14000 mm3 B) Hemoglobin: ≥9.0 g/dL C) Platelet count: ≥100,000 mm3 D) Total Bilirubin: ≤2.0 mg/dL (not apply to cases with obstructive jaundice) E) Creatinine: ≤2.0 mg/dL
  • Ability to understand and the willingness to sign a written informed consent document

Exclusion criteria

  • Planned pancreatogastrostomy
  • Laparoscopic or laparoscope-assisted pancreatoduodenectomy
  • Pancreatic parenchymal atrophy or calcification due to chronic pancreatitis
  • Neoadjuvant treatment including chemotherapy or radiotherapy
  • History of upper abdominal surgery (both of open and laparoscopic) except cholecystectomy
  • Emergency operation
  • Arterial reconstruction such as superior mesenteric artery, common hepatic artery, or celiac artery
  • Severe ischemic heart disease
  • Severe liver dysfunction due to liver cirrhosis or active hepatitis
  • Severe respiratory disorder required oxygen inhalation
  • Chronic renal failure with dialysis
  • Requiring resection of other organs (liver or colon) during pancreatoduodenectomy
  • Immunosuppressive treatment
  • History of severe hypersensitivity to PGA felt and fibrin glue
  • Other severe drug allergies
  • Contrast media allergy of both iodine and gadolinium
  • Active duplicate cancer thought to affect adverse events
  • Severe psychological or neurological disease
  • Drug abuse or alcoholics
  • Planned use of octreotide

Treatment and study plan

PGA felt reinforcement

Drug

During pancreaticojejunostomy, 1) a 0.3 mm thick PGA felt (Neoveil®, Gunze, Japan) is pasted on the ventral side and the dorsal side of pancreatic parenchyma, through which suture between pancreatic parenchyma and jejunum is performed. 2) Before abdominal closure (after completion of all reconstruction, after washing in the abdominal cavity), a 0.15 mm thick PGA felt is further covered around the anastomotic site and fibrin glue is sprayed.

Primary outcomes

  1. Incidence of a clinically relevant POPF (ISGPS grade B/C)

    Time frame: within 3 months after surgery

    Incidence of a clinically relevant POPF (grade B/C), according to the ISGPS criteria which is the evaluation criteria for POPF

Secondary outcomes

  1. Length of drain placement

    Time frame: within 3 months after surgery

    Number of days from operation date to drain removal date (the peripancreatic drain to be removed last)

  2. Length of the hospital stay

    Time frame: within 3 months after surgery

    Number of days from operation date to discharge date

  3. Incidence of overall POPF (Biochemical leak, grade B, and C)

    Time frame: within 3 months after surgery

    Incidence of overall POPF of biochemical leak, grade B, or grade C, according to the ISGPS criteria

  4. Incidence of POPF by each suturing method to approximate the pancreas and the jejunum

    Time frame: within 3 months after surgery

    Incidence of overall POPF of biochemical leak, grade B, or grade C, according to the ISGPS criteria by each suturing method to approximate the pancreas and the jejunum (Kakita, two-layer, or Blumgart)

  5. Incidence of delayed gastric emptying (DGE)

    Time frame: within 3 months after surgery

    Incidence of overall DGE, according to the ISGPS criteria

  6. Incidence of intraabdominal abscess

    Time frame: within 3 months after surgery

    Incidence of intraabdominal abscess of Grade II (requiring pharmacological treatment with drugs) or more, according to Clavien-Dindo classification

  7. Incidence of postpancreatectomy hemorrhage (PPH)

    Time frame: within 3 months after surgery

    Incidence of overall PPH, according to the ISGPS criteria

  8. Incidence of interventional drainage

    Time frame: within 3 months after surgery

    Incidence of additional drainage percutaneously or endoscopically

  9. Incidence of overall postoperative complications

    Time frame: within 3 months after surgery

    Incidence of overall postoperative complications, according to Clavien-Dindo classification

  10. Incidence of POPF-related complications (POPF+DGE+abscess+PPH)

    Time frame: within 3 months after surgery

    Incidence of cases in whom one of 3), 5), 6) or 7) occurred

  11. Incidence of 3-month mortality

    Time frame: within 3 months after surgery

    Incidence of surgery-related deaths from operation date to postoperative 3 months

  12. Incidence of reoperation

    Time frame: within 3 months after surgery

    Incidence of reoperation from operation date to postoperative 3 months

  13. Incidence of readmission

    Time frame: within 3 months after surgery

    Incidence of readmission from operation date to postoperative 3 months

Sponsors and collaborators

Lead sponsor

University of Toyama

Other

Collaborators

  • Gangnam Severance Hospital
  • Kansai Medical University
  • Kumamoto University
  • Nagoya University
  • Nara Medical University
  • National Cancer Center, Korea
  • Osaka City University
  • Osaka University
  • Samsung Medical Center
  • Seoul National University Bundang Hospital
  • Seoul National University Hospital
  • Severance Hospital
  • Shiga Medical University
  • Shimane University
  • Tokyo Medical University
  • Tokyo Medical and Dental University
  • Wakayama Medical University

Registry information

Official study title

PoLyglycolic Acid Felt reiNforcEmenT of the PancreaticoJejunostomy; Multicenter Prospective Randomized Phase III Trial in Japan and Korea (PLANET-PJ Trial)

Important dates

Study start
2018
Primary completion
2021
Study completion
2022
First posted
Nov 6, 2017
Registry last updated
May 5, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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