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CompletedNCT06084975Updated Oct 16, 2023

Comparison of Outcomes Between Warshaw and Kimura Techniques for Spleen-preserving Minimally Invasive Distal Pancreatectomy

An observational study in Distal Pancreatectomy, Spleen Preservation and Postpancreatectomy Hemorrhage, sponsored by Zhejiang University. Completed at 1 site in China. Per ClinicalTrials.gov, last updated 2023-10-16.

Sponsored by Zhejiang University · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
314
Sex
All
01

Study summary

Spleen-persevering distal pancreatectomy (SP-DP) has been widely advocated as a routine procedure for benign or low-grade malignant tumors in the pancreatic body and tail, especially with a minimally invasive approach. Spleen preservation can be accomplished with Kimura technique (KT) or Warshaw technique (WT) Both of the two techniques were proved to be feasible and efficient. However, the perioperative outcomes and long-term benefits between patients with KT and WT in spleen-persevering minimally invasive distal pancreatectomy (SP-MIDP) remains controversial.

Several small series have reported a slightly higher prevalence of postpancreatectomy hemorrhage (PPH) in patients who undergo KT than those undergo WT. The exposure of splenic vessels to erosive pancreatic juice and the preservation of splenic vessels itself may explain the higher chance of PPH in KT. Larger volume studies are warranted to confirm this finding and to clarify the clinical significance. This study compared the perioperative outcomes between the two spleen-preserving techniques, with a focus on parameters relating to perioperative patient safety. Especially, the incidence and clinical relevance of PPH in SP-MIDP were evaluated.

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Conditions studied

  • Distal Pancreatectomy
  • Spleen Preservation
  • Postpancreatectomy Hemorrhage
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In context

Lead sponsor

Zhejiang University is the lead sponsor of 355 studies on the registry; 165 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients who underwent SP-MIDP at our institution between July 2018 and December 2022 were enrolled consecutively.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • pathological diagnosis of benign or low-grade malignant pancreas tumors.

Exclusion criteria

Exclusion Criteria:

  • incomplete medical records,
  • history of previous splenectomy,
  • high-grade malignant pancreas tumors,
  • conversion to open DP (ODP).
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Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
314 participants (actual)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • Kimura technique (KT)

    Spleen preservation is accomplished by sparing the splenic vessels.

    Procedure: Splenic vessels preservation

  • Warshaw technique (WT)

    Spleen preservation is accomplished by sacrificing the splenic vessels and maintaining vascularity through the preserved short gastric and left gastroepiploic vessels.

Interventions

  • ProcedureSplenic vessels preservation

    preservation the splenic vessels

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What researchers measure

Primary outcomes

  1. major complications

    (Clavien-Dindo grade ≥ III)

    Time frame: Within 30 days of SP-MIDP

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Study locations

1 site
  • the First Affiliated Hospital, School of Medicine, Zhejiang University
    Hangzhou, Zhejiang 310003, China
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 16, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06084975
Responsible party
TingBo Liang (Professor, Zhejiang University) — Principal investigator
First posted
Oct 16, 2023
Start date
Jul 1, 2018
Primary completion
Dec 31, 2022
Completion
Dec 31, 2022
Last update
Oct 16, 2023

Study contacts

Liang Tingbo
principal investigator · Zhejiang University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2023. You cannot join it, but the record below documents what was studied.

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