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Intra-abdominal Hypertension and Abdominal Compartment Syndrome in Patients After Pancreatic Procedures.

ConditionsIntra Abdominal PressureAbdominal Compartment SyndromePancreatic SurgeryPancreatic Fistula After PancreaticoduodenectomyDelayed Gastric EmptyingAnastomotic LeaksOverload Fluid
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCharles University, Czech Republic

About this trial

This study investigates the development of intra-abdominal hypertension and compartment syndrome in patients undergoing elective pancreatic procedures. Main objective is to determine the proportion of patients after pancreatic operation who develop elevated intra-abdominal pressure and assess its association with postoperative complication rates. Another goal of the study is to compare open versus robotic pancreatic procedures regarding the occurrence of intra-abdominal hypertension and abdominal compartment syndrome.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients ≥ 18-year-old

Indication for elective pancreatic procedure

Written informed consent

Disqualifiers

Patients <18 years old.

Contraindication for urinary catheter placement.

Refusal to participate in the study.

Trial population

All patients undergoing open or robotic pancreatic procedures in our department.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

150 Participants
are grouped into 1 trial group
Group A: Patients after pancreatic procedures

Trial outcomes

Primary outcomes

1

Prevalence of Intra-abdominal hypertension and abdominal compartment syndrome

Prevalence of intra-abdominal hypertension and abdominal compartment syndrome in patients following pancreatic procedures.

Time frame
From the admission to the intensive care unit until the postoperative day 7 or until discharge from the ICU

Secondary outcomes

1

Correlation between intra-abdominal hypertension and the development of postoperative complications.

The secondary objective aims to explore potential correlations between intra-abdominal hypertension and the development of postoperative complications, such as anastomotic dehiscence, postoperative pancreatic fistulas, prolonged postoperative ileus, or delayed gastric emptying.

Time frame
From the enrollment to the 90 days follow up period.

Other outcomes

1

Incidence of Intra-abdominal hypertension in patients following robotic vs. open pancreatic procedure.

The tertiary objective is to compare open and robotic pancreatic procedures in terms of incidence of intra-abdominal hypertension and ACS

Time frame
From the admission to the intensive care unit for 7 consecutive days or until discharge from the ICU.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Charles University, Czech Republic

Lead sponsor

Military University Hospital, Prague

Collaborator

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: