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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04687826
Other study ID # GDFT1517
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2015
Est. completion date November 20, 2020

Study information

Verified date December 2020
Source Helsinki University Central Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Postoperative complication rates in patients undergoing pancreaticoduodenectomy remain high although the operation techniques have developed a lot in recent years. There is evidence that restrictive intraoperative fluid therapy could decrease postoperative complication rates but the results of the former studies have been somewhat controversial. The aim of this study is to examine whether the intraoperative and postoperative fluid therapy affect to the postoperative complication rates in patients undergoing pancreaticoduodenectomy.


Description:

The study is a retrospective cohort study. The first cohort consists of patients who underwent pancreaticoduodenectomy in year 2015 when intraoperative fluid therapy were managed using goal directed fluid therapy technique. The second cohort consists of patients who underwent pancreaticoduodenectomy in year 2017 when intraoperative fluid therapy were based on the consideration of the anaesthesiologist. In 2015 most of the patients spent the first postoperative night in the ICU where the fluid management and monitoring of the urine output and vital functions were more controlled than in the normal ward. In 2017 most of the patients got in the regular ward right after the surgery. The aim of the study is to examine whether there are differences in the amounts of the intraoperative and postoperative fluids between the cohorts and does the perioperative fluid therapy affect to the complication rates.


Recruitment information / eligibility

Status Completed
Enrollment 168
Est. completion date November 20, 2020
Est. primary completion date December 31, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - age 18 or over - patients who underwent pancreaticoduodenectomy in 2015 or in 2017 Exclusion Criteria: - patients whose patient record information is insufficient

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Goal directed fluid therapy
Patients in 2015 got intraoperative fluid therapy in goal directed fluid therapy technique.
Liberal fluid therapy
Patients in 2017 got liberal intraoperative fluid therapy influenced by their anaesthesiologist.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Helsinki University Central Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Intraoperative fluid volume The amount of fluid (crystalloids and albumin) patients got during the surgery The duration of the surgery
Primary Postoperative complications (Clavien-Dindo classification) The rate of severe Clavien-Dindo complications (3-5) Postoperative day 0-30
Secondary Severe surgical complications The rate of surgical complications (Clavien Dindo 3-5), without cardiopulmonary complications Postoperative day 0-30
Secondary Cardiopulmonary complications The rate of cardiopulmonary complications e.g., congestive heart failure, pleural effusion, dyspnea. Postoperative day 0-30
Secondary Pancreatic fistulas The rate of severe pancreatic fistulas (grade B-C) Postoperative day 0-30
Secondary Postoperative fluid volume The amount of fluid patients got postoperatively Postoperative day 0-3
Secondary Intraoperative fluid balance The change in intraoperative fluid intake (crystalloids, colloids, blood products) and fluid output (urine output, blood loss, evaporation) in millilitres and ml/kg. The duration of the surgery
Secondary Postoperative fluid balance The change in postoperative fluid intake (crystalloids, colloids, blood products) and fluid output (urine output, secretion in drains etc.) in millilitres. Postoperative day 1-3
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