ClinicalTrials.Veeva

Menu

Prolonged Cardiopulmonary Bypass Time as a Predictive Factor for AGI After Heart Valve Replacement

H

Hepatopancreatobiliary Surgery Institute of Gansu Province

Status

Completed

Conditions

Heart Valve Diseases

Treatments

Other: CPB time

Study type

Observational

Funder types

Other

Identifiers

NCT05498935
CPB-AGI

Details and patient eligibility

About

In this retrospective study, the investigators will analyze the correlation between cardiopulmonary bypass (CPB) time and acute gastrointestinal injury (AGI), and the outcomes of AGI in patients undergoing heart valve replacement.

Full description

Patients with heart valve diseases often have chronic cardiac insufficiency. Patients undergoing heart valve replacement with CPB are always complicated with gastrointestinal tract ischemia-reperfusion injury, which usually leads to AGI. AGI after cardiovascular surgery, especially in that use CPB, is associated with significant morbidity and an increase in peri-operative mortality. Prolonged CPB time could be predictive of AGI following heart valve replacement. This study is to analyze the correlation between CPB time and AGI, and the outcomes of AGI in patients undergoing heart valve replacement. The investigators hope that the benefits will include fewer patients becoming seriously postoperative AGI and mortality after cardiac surgery.

Enrollment

1,070 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing heart valve replacement surgery with CPB
  • Age > 18 years and ≤ 70 years

Exclusion criteria

  • Patients combined with severe hematological disease, respiratory disease, and other critical diseases
  • Patients had severe disorder of multiple systems and organs or severe pulmonary hypertension
  • Have received major gastrointestinal surgery within 5 years
  • Inflammatory bowel disease (IBD), including ulcerative colitis, Crohn's disease, or colitis
  • Acute gastroenteritis
  • Clostridium difficile or Helicobacter pylori infection
  • Chronic constipation
  • Peptic ulcer
  • Polyps in the stomach or intestines
  • Gastrointestinal neoplasms
  • Abdominal hernia
  • Irritable bowel syndrome
  • Acute or chronic cholecystitis, hepatitis
  • Patients who died during surgery
  • Patients with digestive system tumors

Trial design

1,070 participants in 2 patient groups

CPB time ≥ 90 minutes
Description:
No intervention, regular therapy
Treatment:
Other: CPB time
CPB time < 90 minutes
Description:
No intervention, regular therapy
Treatment:
Other: CPB time

Trial contacts and locations

1

Loading...

Central trial contact

Wenbo Meng, M.D. Ph.D

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems