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Effect of the Heidelberg interprofessional training ward on quality of care vs. care on a regular surgical ward in abdominal surgery - a open randomized controlled non-inferiority trial (HIPSTA-trial)

Effect of the Heidelberg interprofessional training ward on quality of care vs. care on a regular surgical ward in abdominal surgery - a open randomized controlled non-inferiority trial (HIPSTA-trial) - HIPSTA trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00018951
Enrollment
198
Registered
2019-10-23
Start date
2021-02-03
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Scheduled elective abdominal surgery

Interventions

Sponsors

Universitätsklinikum Heidelberg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: For patients (Part I, RCT): - Patients scheduled for elective abdominal surgery - Ability of subject to understand character and individual consequences of the study - Written informed consent - Age =18 years

Exclusion criteria

Exclusion criteria: For patients (Part I, RCT): - American Association of Anesthesiologists (ASA) grade > 3 - Pregnant or lactating women - Language barrier that impedes follow-up - Participation in another intervention-trial with interference of intervention and outcome of this study

Design outcomes

Primary

MeasureTime frame
Comprehensive complication index until postoperative day 30.

Secondary

MeasureTime frame
1. Patient’s perspective of hospital care measured via the patient-reported outcome measurement (PROM) HCAHPS (Hospital Consumer Assessment of Healthcare Providers and System) 1 month after discharge 2. Length of hospital stay (in days) 3. Rate of readmissions within 1 month after discharge 4. Average number of steps per day measured via a pedometer during the first 4 days on the regular ward 5. Rate of superficial and deep surgical site infections (SSI) 6. Rate of deep vein thrombosis (DVT) until discharge 7. Rate of postoperative lower respiratory tract infections (clinically defined pneumonia or bronchitis, tracheobronchitis, tracheitis) until discharge 8. Rate of urinary tract infections (symptomatic urinary tract infection OR asymptomatic bacteriuria with secondary sepsis) until discharge 9. Rate of primary sepsis as defined by current sepsis guidelines (sepsis-3) until discharge 10. Rate of pulmonary embolisms diagnosed via chest CT until discharge 11. Rate of catheter related infections (arterial and venous infections) until discharge

Countries

Germany

Contacts

Public ContactAndré Mihaljevic

Klinik für Allgemein-, Viszeral- und TransplantationschirurgieUniversitätsklinikum Heidelberg

andre.mihaljevic@med.uni-heidelberg.de06221-5636986

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026