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CardiosurgeryNCT06080295

The Kallikrein-Kinin System in Cardiac Surgery

An observational study of Cardiosurgery, run by Qin Zhang at 1 site in China.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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 more about this study

Who is it for?
Ages 18 to 80 years
Conditions the study is for
Cardiosurgery
How many people
287 participants
Where
1 siteChina
Study dates
20 Sep 2023to 30 Sep 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

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).

Who may be able to join

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

Who cannot join

  • Patients meeting any of the following criteria were excluded from the study:
  • 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.
  • Surgical and Systemic Factors:
Show all 12Show fewer
  • 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.
  • Pharmacological Factors:
  • Administration of nitrates after hospital admission (due to potential confounding effects on endothelial function and nitric oxide signaling).

Trial locations and contacts

1 site in 1 country.

China1 site
  • Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology

    Wuhan, Hubei, 430030

Other trials in China

About this study

Official title: The Involvement of the Kallikrein-Kinin System in the Pathogenesis of Postoperative Injury in Cardiac Surgery: An Observational Study

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.

Conditions
Cardiosurgery
Keywords
KKS; tissue kallikrein; ;cardiosurgery;cardiopulmonary bypass

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. KLK1 level

    KKS related factors levels

    Measured: 24 hours

  2. POD-postoperative delirium

    Confusion Assessment Method for the ICU (CAM-ICU)

    Measured: 7 days

Secondary outcomes (2)
  1. survival

    survival and clinical symptom

    Measured: 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.

    Measured: 24 hours

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 Oct 2023
  2. Study start20 Sep 2023
  3. Primary completion30 Sep 2025
  4. Study completion30 Sep 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
287 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06080295
Sponsor's protocol ID
TJ-IRB20230932
Status last verified
May 2026
First submitted
6 Oct 2023
Last updated
18 May 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Cardiosurgery, run by Qin Zhang at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 12 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 18 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

KLK1 level (time frame: 24 hours). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 May 2026.

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