NCT07396662

Brief Summary

Pancreatic diseases often require surgery or invasive procedures to provide a chance for a cure. However, due to the pancreas's unique anatomical structure, its relative position to adjacent organs, and its dual endocrine and exocrine functions, the complexity of surgery is increased, impacting the patient's postoperative quality of life. Therefore, this project aims to retrospectively collect basic data, preoperative and postoperative blood tests (blood cell counts, biochemistry, tumor markers, glucose-related, lipid-related), and preoperative and postoperative imaging examinations (CT, MRI, Ultrasound, PET scan, Endoscopy, etc.) of patients who underwent pancreatic surgery at our hospital. We aim to compare whether surgical methods, lesion margin clearance rates, and postoperative remnant pancreatic volume affect the patient's endocrine function, exocrine function, quality of life, and disease prognosis. This analysis is intended to understand the indications, surgery-related factors, and prognosis for patients planning to undergo pancreatic surgery, with the expectation of providing more diverse and specific treatment recommendations for patients with pancreatic diseases in the future

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
3,500

participants targeted

Target at P75+ for all trials

Timeline
104mo left

Started Jan 2016

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress55%
Jan 2016Dec 2034

Study Start

First participant enrolled

January 1, 2016

Completed
10.1 years until next milestone

First Submitted

Initial submission to the registry

January 22, 2026

Completed
18 days until next milestone

First Posted

Study publicly available on registry

February 9, 2026

Completed
8.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2034

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2034

Last Updated

February 9, 2026

Status Verified

January 1, 2026

Enrollment Period

19 years

First QC Date

January 22, 2026

Last Update Submit

February 5, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • postoperative pancreatic endocrine-exocrine functions

    1. Pancreatic endocrine function will be measured by incidence of appearance of new-onset or aggravated DM after operation. 2. pancreatic exocrine function will be measured by incidence of appearance of steatorrhea which can be alleviated by replacement of digestive enzyme.

    6 months after pancreatectomy

Study Arms (1)

pancreatectomy group

Procedure: pancreatectomy

Interventions

all procedures demanding pancreatic parenchyma transaction

pancreatectomy group

Eligibility Criteria

Age20 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

All patients received pancreatectomy at National Taiwan University Hospital after 2017

You may qualify if:

  • All patients scheduled for pancreatectomy

You may not qualify if:

  • Age under 20 years or older than 75 years; Pregnancy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Taiwan University Hospital

Taipei, Taiwan, 10002, Taiwan

RECRUITING

MeSH Terms

Conditions

Pancreatic Neoplasms

Interventions

Pancreatectomy

Condition Hierarchy (Ancestors)

Digestive System NeoplasmsNeoplasms by SiteNeoplasmsEndocrine Gland NeoplasmsDigestive System DiseasesPancreatic DiseasesEndocrine System Diseases

Intervention Hierarchy (Ancestors)

Digestive System Surgical ProceduresSurgical Procedures, Operative

Central Study Contacts

Yu Wen Tien, Ph.D.

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Clinical Professor

Study Record Dates

First Submitted

January 22, 2026

First Posted

February 9, 2026

Study Start

January 1, 2016

Primary Completion (Estimated)

December 31, 2034

Study Completion (Estimated)

December 31, 2034

Last Updated

February 9, 2026

Record last verified: 2026-01

Locations