Randomized control study of the usability of vessel sealing devices at the time of pancreatoduodenectomy

Randomized control study of the usability of vessel sealing devices at the time of pancreatoduodenectomy - Randomized control study of the usability of vessel sealing devices at the time of pancreatoduodenectomy

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000023311

Enrollment

100

Registered

2016-07-26

Start date

2016-07-26

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Diseases which required pancreas head resection

Interventions

LigaSure Small Jaw produced by COVIDIEN JAPAN Intervention during operation time of pancreatoduodenectomy Harmonic FOCUS produced by Johnson and Johnson Intervention during operation time of pancrea

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: #1 20 years old or more at the time of agreement of participation for this study. #2 Patients who understood well about this study and agreed to the participation for this study.

Exclusion criteria

Exclusion criteria: #1Unresectable cases after registration to this study #2patients who have liver cirrhosis #3Patients who required anti coagulation therapy during perioperative time. #4patients who was considered as inadequate by principal researcher

Design outcomes

Primary

Measure	Time frame
Subjective evaluation of sealing devices by surgeon (questionnaire survey)	—

Secondary

Measure	Time frame
1.Operative time and intra-operative blood loss 2.Postoperative complications 3.Quantity of drainaged fluid at postoperative day 1 and 2.	—

Countries

Japan

Contacts

Public ContactSohei Satoi

Kansai Medical University Surgery

satoi@hirakata.kmu.ac.jp0728041010

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026