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Completed

NCT Number: NCT04483726

Distal Pancreatectomy, Minimally Invasive or Open, for Malignancy (DIPLOMA)

Objective: To compare MIDP with ODP regarding radical resection rate for pancreatic ductal adenocarcinoma (PDAC) in the pancreatic body or tail.

Study design: A pan-European, randomized controlled, multicenter, patient-blinded non-inferiority trial. This protocol was designed according to the SPIRIT guidelines1. Pathologists judging the primary endpoint will be blinded for the surgical approach (MIDP vs ODP). A blinded adjudication committee will assess all endpoints.

Study population: Two groups of 129 patients (258 in total) with an indication for elective distal pancreatectomy with splenectomy because of proven or highly suspected PDAC.

Intervention: Minimally invasive distal pancreatectomy (either laparoscopic or robot-assisted)

Control: Open distal pancreatectomy

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hôpital Beaujon - APHP, Clichy, France

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About this study

Rationale: Several systematic reviews have suggested superior short term outcomes after minimally invasive distal pancreatectomy (MIDP) as compared to open distal pancreatectomy (ODP) for benign and pre-malignant disease. In the literature and in a recent pan-European survey, about one third of pancreatic surgeons expressed concerns regarding the oncologic safety (i.e. radical resection, lymph node retrieval and survival) of MIDP in pancreatic cancer. Most surgeons stated that a randomized trial assessing oncologic safety in MIDP vs ODP for pancreatic cancer is needed.

Objective: To compare MIDP with ODP regarding radical resection rate for pancreatic ductal adenocarcinoma (PDAC) in the pancreatic body or tail.

Study design: A pan-European, randomized controlled, multicenter, patient-blinded non-inferiority trial. This protocol was designed according to the SPIRIT guidelines1. Pathologists judging the primary endpoint will be blinded for the surgical approach (MIDP vs ODP). A blinded adjudication committee will assess all endpoints.

Study population: Two groups of 129 patients (258 in total) with an indication for elective distal pancreatectomy with splenectomy because of proven or highly suspected PDAC.

Intervention: Minimally invasive distal pancreatectomy (either laparoscopic or robot-assisted)

Control: Open distal pancreatectomy

Main study parameters/endpoints: Primary outcome is the microscopically radical (R0, >1mm) resection rate. Main secondary outcomes are survival, lymph node retrieval, intraoperative outcomes (such as blood loss, operative time and conversion), postoperative outcomes (such as complications, time to functional recovery and hospital stay) and quality of life

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • ≥ 18 years;
  • Elective indication for distal pancreatectomy for proven or suspected PDAC;
  • Upfront (without induction / down-sizing radio- and/or chemotherapy) resectable PDAC in the pancreatic body or tail;
  • The tumor can be radically resected via both minimally invasive or open surgery according to the local treating team;
  • The patient is fit to undergo both open and minimally invasive distal pancreatectomy

Exclusion criteria

  • score of American society of anaesthesiologists (ASA) >3;
  • A medical history of chronic pancreatitis (according to the M-ANNHEIM criteria);
  • Second malignancy necessitating resection during the same procedure;
  • Distant metastases (M1) including involved distant lymph nodes;
  • Tumor involvement or abutment of major vessels (celiac trunk*, mesenteric artery or portomesenteric vein);
  • Pregnancy;
  • Participation in another study with interference of study outcomes.
  • Cystic lesion having undergone malignant transformation
  • the celiac trunk should be 5mm clear from tumor

Treatment and study plan

Minimally invasive distal pancreatectomy

Procedure

Minimally invasive distal pancreatectomy (either laparoscopic or robot-assisted)

open distal pancreatectomy

Procedure

open distal pancreatectomy

Primary outcomes

  1. microscopically radical resection rate

    Time frame: 1 day

    R0, >1mm

Secondary outcomes

  1. survival

    Time frame: 1 year

    Date of death

  2. survival

    Time frame: 2 years

    Date of death

  3. survival

    Time frame: 3 years

    Date of death

  4. lymph node retrieval

    Time frame: 1 day

    Tumor positive lymph nodes retrieved

  5. Operative time

    Time frame: 1 day

    Operative time from first incision to closure of the abdomen, minutes

  6. Intraoperative blood loss

    Time frame: 1 day

    Intraoperative blood loss, mL (suction canister and weight of gauzes)

  7. intraoperative outcomes

    Time frame: 1 day

    Total duration of the procedure, minutes

  8. postoperative outcomes

    Time frame: 1 day

    Major complications

  9. specimen size

    Time frame: 1 day

    Tumor size, mm

  10. Specimen length

    Time frame: 1 day

    Specimen length, mm

  11. margin

    Time frame: 1 day

    Distance from tumor to transection, anterior and posterior margin, mm

Sponsors and collaborators

Lead sponsor

University Hospital, Montpellier

Other

Collaborators

  • AIDS Malignancy Consortium

Registry information

Official study title

Distal Pancreatectomy, Minimally Invasive or Open, for Malignancy (DIPLOMA): a Pan-European, Randomized Controlled, Multicenter, Patient Blinded, Non-inferiority Trial

Acronym: DIPLOMA

Important dates

Study start
2020
Primary completion
2021
Study completion
2024
First posted
Jul 23, 2020
Registry last updated
Jun 22, 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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