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

C

Charles University, Czech Republic

Status

Not yet enrolling

Conditions

Intra Abdominal Pressure
Overload Fluid
Pancreatic Surgery
Abdominal Compartment Syndrome
Delayed Gastric Emptying
Pancreatic Fistula After Pancreaticoduodenectomy
Anastomotic Leaks

Study type

Observational

Funder types

Other

Identifiers

NCT06672601
108/19-61/2024

Details and patient eligibility

About

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.

Full description

HYPA study is designed as a prospective observational study. The primary objective of this study is to assess the risk and prevalence of intra-abdominal hypertension and abdominal compartment syndrome following pancreatic procedures. 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. The third objective is to compare the incidence of intra-abdominal hypertension in patients undergoing robotic versus open pancreatic procedures

Enrollment

150 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients ≥ 18-year-old
  • Indication for elective pancreatic procedure
  • Written informed consent

Exclusion criteria

  • Patients <18 years old.
  • Contraindication for urinary catheter placement.
  • Refusal to participate in the study.

Trial design

150 participants in 1 patient group

Patients after pancreatic procedures
Description:
All patients following pancreatic procedure

Trial contacts and locations

1

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Central trial contact

Štěpán-Ota Schütz, MD.

Data sourced from clinicaltrials.gov

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