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Study identifier: NCT06381427 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: RecruitingPeriOP-CARE HF

Perioperative Interdisciplinary, Intersectoral Process Optimization in Heart Failure

Condition: Heart Failure  ·  Sponsor: University of Giessen

PhaseNA
Planned participants1057
Who can joinAll sexes, 65 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
WhereGiessen, Germany

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

Chronic heart failure affects up to three million people in Germany, with prevalence increasing with age. It is a leading cause of cardiovascular disease-related deaths. Patients with heart failure undergoing non-cardiac surgery face higher risks of complications and death compared to those with coronary artery disease. Despite guidelines recommending comprehensive preoperative evaluation, there is no systematic risk assessment structure in place, leading to inadequate perioperative care. This study aims to evaluate a multidisciplinary approach for high-risk patients aged 65 and above, regardless of prior heart failure diagnosis, to mitigate postoperative complications. The investigators measure the NTpro BNP before surgery and include patients with NTproBNP\> 450 in this study and randomize them either to the standard care group or the intervention group.The hypothesis is that standardized risk screening and multidimensional care (Intervention group) can reduce complications in these patients undergoing non-cardiac surgery.

This description comes directly from the study's public registry record.

Talk to the study team

Götz Schmidt, MD  ·  +4964198544401  ·  goetz.f.schmidt@chiru.med.uni-giessen.de

Marit Habicher, MD  ·  +4964198544401

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Age ≥ 65 years * Elective non-cardiac surgical operation with intermediate or high operative risk under general anesthesia or combined anesthesia (general and regional anesthesia) as per Figure 1 * ASA (American Society of Anesthesiologists) grade ≥ II * Qualification for randomization: NT-proBNP ≥ 450pg/ml during routine preoperative evaluation and anesthesia consultation. Exclusion Criteria: * Age \< 65 years * Cardiac surgery and cardiology interventional procedures * Transplantation surgery (e.g., kidney, liver, lung transplantation) * Kidney surgery (e.g., nephrectomy, partial nephrectomy) * Procedures involving cardiopulmonary bypass * Emergency surgery * Surgery under general anesthesia within the last 30 days * Primary use of local or regional anesthesia * Chronic kidney insufficiency with eGFR \< 15 ml/min or dialysis-dependent kidney insufficiency * Surgical time \< 30 minutes * Participation in another interventional study * Lack of consent * Limited language proficiency * Patient's limited or absent capacity to provide consent, as well as patients under legal guardianship

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (1)

Justus Liebig University Giessen, University Hospital Giessen and MarburgGiessen, GermanyRecruiting

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Giessen

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