NCT03060408

Brief Summary

In this retrospective cohort study, the investigators reviewed and analyzed the electronic medical records of consecutive patients who underwent distal pancreatectomy either via laparotomy or laparoscopy. Intraoperative fluid administration amount, postoperative complications, length of hospital stay, and readmission rate were evaluated. The total fluid amounts were calculated using the sum of colloids multiplied by 1.5 or 2.0 and crystalloids.

Trial Health

100
On Track

Trial Health Score

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

Enrollment
304

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jun 2016

Shorter than P25 for all trials

Status
completed

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 Start

First participant enrolled

June 1, 2016

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2016

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

January 31, 2017

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2017

Completed
22 days until next milestone

First Posted

Study publicly available on registry

February 23, 2017

Completed
Last Updated

February 23, 2017

Status Verified

February 1, 2017

Enrollment Period

6 months

First QC Date

January 31, 2017

Last Update Submit

February 21, 2017

Conditions

PancreatectomyFluid TherapyLaparoscopy

Keywords

Fluid TherapyLaparoscopy

Outcome Measures

Primary Outcomes (1)

  • intraoperatively administered fluid amounts

    one year

Study Arms (2)

Open

Patients underwent open distal pancreatectomy

Laparoscopic

Patients underwent laparoscopic distal pancreatectomy

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

indication of distal pancreatectomy

You may qualify if:

  • indication of distal pancreatectomy

You may not qualify if:

  • transfusion
  • ASA physical status over 4
  • co-operate other surgery

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator, Resident of Anesthesiology and Pain medicine

Study Record Dates

First Submitted

January 31, 2017

First Posted

February 23, 2017

Study Start

June 1, 2016

Primary Completion

December 1, 2016

Study Completion

February 1, 2017

Last Updated

February 23, 2017

Record last verified: 2017-02