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RecruitingNCT05128890Updated Mar 20, 2026

Evaluation of Resection Techniques for Pancreatic Tumors

An observational study in Surgery, Liver Tumor and Pancreas Tumor, sponsored by Methodist Health System. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-03-20.

Sponsored by Methodist Health System · Observational

From the registry’s dates

  • Started Apr 2016; still recruiting 10 years 5 months later.
Study type
Observational
Model
Other
Time perspective
Retrospective
Enrollment
431
Ages
18 Years and older
Sex
All
01

Study summary

The objective of this study is to compare open and minimally invasive pancreatic and liver resection techniques and analyze the different outcome variables from the clinical standpoint.

The plan is to investigate patient survival, length of stay, complication rates, operative time, transfusion rate, 30 and 90-day readmission rate, and hospital charges.

Read the detailed description

The plan is to conduct a retrospective chart review of patients who have undergone pancreatic and liver resection by using Meditech and Epic. A non-identified database will be created after retrospectively reviewing each patient case involving pancreatic or liver resection at MDMC. The study period will start in January 2006 until December 2020. Variables will include demographics, clinical disease diagnoses, and operative parameters as well as indirect charges from the hospitalizations.

02

Conditions studied

  • Surgery
  • Liver Tumor
  • Pancreas Tumor
03

In context

Carcinoma, Hepatocellular

3,182 studies on the registry are indexed under Carcinoma, Hepatocellular; 954 are open to participants now.

This study's planned enrollment of 431 is above the median of 200 across 754 observational studies indexed under Carcinoma, Hepatocellular.

Browse Carcinoma, Hepatocellular studies →

Lead sponsor

Methodist Health System is the lead sponsor of 169 studies on the registry; 52 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

pancreatic or liver resection surgeries from January 2006 until December 2020 at Methodist Dallas Medical Center (MDMC)

Inclusion criteria

  • Patients that have undergone pancreatic or liver resection surgeries from January 2006 until December 2020 at Methodist Dallas Medical Center (MDMC)
  • Patients 18 years old or older

Exclusion criteria

Exclusion Criteria:

  • Patients that have not undergone pancreatic resection surgeries
  • Patients under 18 years of age
05

Study design

Observational model
Other
Time perspective
Retrospective
Enrollment
431 participants (estimated)
Patient registry
No

Interventions

  • ProcedureResection techniques for pancreatic and liver tumors

    to compare open versus minimally invasive pancreatic resection techniques and analyze the different outcome variables from the clinical standpoint

    Also known as: minimally invasive pancreatic resection techniques

06

What researchers measure

Primary outcomes

  1. Patient Survival

    It will be calculated in days.Minimally invasive techniques are being adopted for complex pancreatic and liver surgery and there is a need to understand if these techniques are advantageous to the patient, if the cost is justified and if the risks are acceptable when compared to the gold standard open surgery.

    Time frame: through study completion, an average of 1 year

  2. Length of stay

    It will be calculated in days. The days stayed in hospital post-procedure.

    Time frame: Up to 1 year

  3. Complication rates

    Patient may visit physician or hospital for any symptoms or may need hospitalizations.

    Time frame: through study completion, an average of 1 year

  4. Operative time

    The time required for the procedure.

    Time frame: up to 10 hours

  5. Transfusion rate

    If any post-procedure transfusion required, will be recorded.

    Time frame: through study completion, an average of 1 year

  6. 30 and 90 day readmission rate

    After the procedure any hospital admissions up to 30 days will be recorded.

    Time frame: through study completion, an average of 1 year

  7. Hospital charges

    The hospital charges for the procedure will be recorded.

    Time frame: through study completion, an average of 1 year

07

Study locations

1 of 1 sites recruiting
  • Methodist Dallas Medical Center
    Dallas, Texas 75203, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 20, 2026, 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
NCT05128890
Lead sponsor
Methodist Health System
Responsible party
Sponsor
First posted
Nov 22, 2021
Start date
Apr 16, 2016
Primary completion
Apr 26, 2027 (estimated)
Completion
Apr 26, 2027 (estimated)
Last update
Mar 20, 2026

Study contacts

Colette N Ndjom, MS
Contact
ClinicalResearch@mhd.com
214-947-4681 ext. 74681
Jennifer Kirchner
Contact
jenniferkirchner@mhd.com
214-947-4459 ext. 74459
Alejandro Mejia, M.D.
principal investigator · The Liver Institute, Methodist Dallas Medical Center

Oversight

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

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