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CompletedNCT06080295Updated May 18, 2026

The Kallikrein-Kinin System in Cardiac Surgery

An observational study in Cardiosurgery, sponsored by Qin Zhang. Completed at 1 site in China. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-05-18.

Sponsored by Qin Zhang · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
287
Ages
18 Years to 80 Years
Sex
All
01

Study summary

We aimed to established an interlink among the kallikrein-kinin system (KKS), endothelial dysfunction and POD in response to cardiosurgery , using clinic investigation.

Read the detailed description

This prospective, single-center observational study enrolled 287 adult patients undergoing elective cardiac surgery between October 2023 and September 2025. Plasma samples were collected at three predefined time points: preoperatively, immediately after surgery, and 24 hours post-surgery. Clinical follow-up for delirium assessments was performed for up to seven days postoperatively or until hospital discharge.

Participants In this prospective, observational cohort study, consecutive adult patients (aged ≥18 years) scheduled for elective cardiac surgery requiring CPB-including open-heart valve repair or replacement-were screened for eligibility between October 2023 and September 2025. Absolute exclusion criteria were strictly defined as follows: 1) pregnancy; 2) preoperative cognitive impairment, preexisting delirium, or a history of severe psychiatric disorders (e.g., dementia, schizophrenia, major depressive disorder) with significant psychotropic medication use; 3) major neurological disorders, including a history of stroke, severe cerebrovascular disease, or severe traumatic brain injury within the past six months; 4) emergent or salvage surgery; 5) severe hepatic or renal dysfunction requiring dialysis; 6) current systemic infection or severe immunosuppression; and 7) administration of nitrates after hospital admission.

During the screening phase, patients who met the predefined exclusion criteria, lacked incomplete perioperative plasma sampling, or declined to provide informed consent were excluded. Ultimately, a final cohort of 287 eligible patients was enrolled in the study . Based on their intraoperative clinical management, the enrolled patients were categorized into the ulinastatin treatment group (n = 123) and the untreated control group (n = 164).

Adult patients undergoing elective cardiac surgery, including open-heart valve repair, valve replacement with cardiopulmonary bypass (CPB) were consecutively screened for eligibility between October 2023 and September 2025. Patients were excluded if they were ≤18 years old, pregnant, had preexisting POD or a history of psychiatric disorders such as schizophrenia or major depressive disorder, had a significant history of psychotropic medication use, received nitrates after admission, or had major neurological disorders including severe traumatic brain injury or stroke within the past six months.

Variables and Clinical Outcomes Preoperative baseline variables, including patient demographics and comorbidities, were systematically extracted from electronic health records. To evaluate the systemic inflammatory and organ injury status, peak postoperative cTnI and lactate Lac levels were recorded as secondary clinical endpoints. Simultaneously, serial perioperative plasma KLK1 levels were quantified as the primary mechanistic and predictive biomarker. The primary clinical outcome was the incidence of POD within 7 days post-surgery. Delirium was assessed twice daily using the Confusion Assessment Method for the ICU (CAM-ICU) or the 3D-CAM by trained evaluators who were strictly blinded to the patients' clinical exposure and biomarker data.

02

Conditions studied

  • Cardiosurgery

Keywords

  • KKS; tissue kallikrein; ;cardiosurgery;cardiopulmonary bypass
03

In context

Lead sponsor

Qin Zhang is the lead sponsor of 12 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

In this prospective, observational cohort study, consecutive adult patients (aged ≥18 years) scheduled for elective cardiac surgery requiring cardiopulmonary bypass (CPB)-including open-heart valve repair or replacement-were screened for eligibility between October 2023 and September 2025.

During the screening phase, patients who met the predefined exclusion criteria, had incomplete perioperative plasma sampling, or declined to provide informed consent were excluded. Ultimately, a final cohort of 287 eligible patients was enrolled in the study . Based on their intraoperative clinical management, the enrolled patients were categorized into the ulinastatin treatment group (n = 123) and the untreated control group (n = 164).

Inclusion criteria

  1. Patients were eligible for enrollment if they met all of the following criteria:
  2. Adult patients aged 18 years or older.
  3. Scheduled for elective cardiac surgery requiring cardiopulmonary bypass (CPB), specifically including open-heart valve repair or replacement.
  4. Provided written informed consent from the patient or a legally authorized representative.

Exclusion criteria

Exclusion Criteria

Patients meeting any of the following criteria were excluded from the study:

  1. Neurological and Psychiatric Factors:

    Preoperative cognitive impairment or preexisting delirium.

    History of severe psychiatric disorders (e.g., schizophrenia, major depressive disorder) requiring significant psychotropic medication use.

    Major neurological disorders, including a history of stroke, severe cerebrovascular disease, or severe traumatic brain injury within the past six months.

  2. Surgical and Systemic Factors:

    Scheduled for emergent or salvage cardiac surgery.

    Severe hepatic or renal dysfunction requiring dialysis.

    Current systemic infection, sepsis, or a state of severe immunosuppression.

    Pregnant or lactating women.

  3. Pharmacological Factors:

Administration of nitrates after hospital admission (due to potential confounding effects on endothelial function and nitric oxide signaling).

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
287 participants (actual)
Patient registry
No
Biospecimen retention
Samples without dna
06

What researchers measure

Primary outcomes

  1. KLK1 level

    KKS related factors levels

    Time frame: 24 hours

  2. POD-postoperative delirium

    Confusion Assessment Method for the ICU (CAM-ICU)

    Time frame: 7 days

Secondary outcomes

  1. survival

    survival and clinical symptom

    Time frame: 7 days

  2. Left Ventricular Ejection Fraction (LVEF) assessed by echocardiography.

    LVEF will be measured using the Simpson's method to evaluate the systolic function of the heart.

    Time frame: 24 hours

07

Study locations

1 site
  • Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
    Wuhan, Hubei 430030, China
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06080295
Lead sponsor
Qin Zhang
Responsible party
Qin Zhang (phd, Tongji Hospital) — Sponsor-investigator
First posted
Oct 12, 2023
Start date
Sep 20, 2023
Primary completion
Sep 30, 2025
Completion
Sep 30, 2025
Last update
May 18, 2026

Study contacts

Qin Zhang, phd
principal investigator · Tongji Hospital

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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