CardiosurgeryNCT06080295
The Kallikrein-Kinin System in Cardiac Surgery
An observational study of Cardiosurgery, run by Qin Zhang at 1 site in China.
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
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.
KLK1 level
KKS related factors levels
Measured: 24 hours
POD-postoperative delirium
Confusion Assessment Method for the ICU (CAM-ICU)
Measured: 7 days
Secondary outcomes (2)
survival
survival and clinical symptom
Measured: 7 days
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.
- First posted12 Oct 2023
- Study start20 Sep 2023
- Primary completion30 Sep 2025
- Study completion30 Sep 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for CardiosurgeryStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Qin Zhang
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Qin Zhang, Tongji Hospital
- Investigators
- Qin Zhang, phd, Principal investigator, Tongji Hospital
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
Study at a glance
From the registry record, last updated by the sponsor on 18 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Involvement of the Kallikrein-Kinin System in the Pathogenesis of Postoperative Injury in Cardiac Surgery: An Observational Study
- ClinicalTrials.gov ID
- NCT06080295
- Acronym / sponsor ID
- TJ-IRB20230932
- Conditions
- Cardiosurgery
- Keywords
- KKS; tissue kallikrein; ;cardiosurgery;cardiopulmonary bypass
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 287 participants (actual)
- Lead sponsor
- Qin ZhangUniversity, hospital or other
- Study start
- 20 Sep 2023 (actual)
- Primary completion
- 30 Sep 2025 (actual)
- Study completion
- 30 Sep 2025 (actual)
- First posted
- 12 Oct 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
We aimed to established an interlink among the kallikrein-kinin system (KKS), endothelial dysfunction and POD in response to cardiosurgery , using clinic investigation.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 to 80 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- 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).
Key inclusion criteria (4 listed)
- 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.
Key exclusion criteria (12 listed)
- 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:
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
KLK1 level
Time frame: 24 hours
KKS related factors levels
POD-postoperative delirium
Time frame: 7 days
Confusion Assessment Method for the ICU (CAM-ICU)
2 secondary outcomes
survival
Time frame: 7 days
Left Ventricular Ejection Fraction (LVEF) assessed by echocardiography.
Time frame: 24 hours
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 May 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Qin Zhang, phd principal investigator
Tongji Hospital
1 site in 1 country: see every site and its status.
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.