NCT07012668

Brief Summary

The objective of this observational cohort study is to evaluate the clinical outcomes of various treatment strategies for cerebrovascular and cardiovascular diseases. Furthermore, it aims to investigate the factors that influence adverse outcomes from these treatments.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,000

participants targeted

Target at P75+ for all trials

Timeline
17mo left

Started Sep 2024

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress54%
Sep 2024Sep 2027

Study Start

First participant enrolled

September 19, 2024

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

June 1, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

June 10, 2025

Completed
2.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 19, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 19, 2027

Last Updated

June 12, 2025

Status Verified

June 1, 2025

Enrollment Period

3 years

First QC Date

June 1, 2025

Last Update Submit

June 9, 2025

Conditions

Keywords

Neuro-co-cardiological diseasesPost-cardiac surgery Cerebrovascular diseasesSimultaneous treatmentStaged treatmentConservative treatment

Outcome Measures

Primary Outcomes (1)

  • Modified Rankin Scale Score

    Modified Rankin Scale(0-6), A lower MRS score indicates better functional status for the patient.

    90±7 days

Secondary Outcomes (7)

  • Modified Rankin Scale Score

    7±1 days or the day discharged

  • Modified Rankin Scale Score

    365±30 days

  • Perioperative complication rate

    30±7 days

  • Rate of cardiovascular and cerebrovascular events

    90±7 days

  • Rate of cardiovascular and cerebrovascular events

    365±30 days

  • +2 more secondary outcomes

Study Arms (5)

Neuro-co-cardiological diseases: Simultaneous treatment

Simultaneous interventional therapy/Simultaneous surgical treatment/ Simultaneous hybrid surgical treatment

Procedure: Interventional or surgical treatment

Neuro-co-cardiological diseases: Staged treatment

Staged interventional therapy/Staged surgical treatment/Staged hybrid surgical treatment

Procedure: Interventional or surgical treatment

Neuro-co-cardiological diseases: Conservative treatment

Surgery/intervention for one disease and conservative treatment for another disease or Simultaneously conservative treatment

Post-cardiac surgery Cerebrovascular disease: Surgery/Interventional Treatment

Post-cardiac surgery Cerebrovascular disease: Surgery/Interventional Treatment

Procedure: Interventional or surgical treatment

Post-cardiac surgery Cerebrovascular disease: Conservative treatment

Post-cardiac surgery Cerebrovascular disease: Conservative treatment

Interventions

Simultaneous interventional or surgical treatment/staged interventional or surgical treatment

Neuro-co-cardiological diseases: Simultaneous treatmentNeuro-co-cardiological diseases: Staged treatment

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients with neuro-co-cardiological diseases or post-cardiac surgery cerebrovascular diseases

You may qualify if:

  • Age ≥18 years;
  • Patients with neuro-co-cardiological diseases or post-cardiac surgery cerebrovascular diseases.

You may not qualify if:

  • The expected survival is less than 1 years;
  • Simultaneously merge other serious diseases;

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Beijing Anzhen Hospital

Beijing, China

RECRUITING

MeSH Terms

Interventions

MethodsSurgical Procedures, Operative

Intervention Hierarchy (Ancestors)

Investigative Techniques

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
OTHER
Target Duration
1 Year
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Prof

Study Record Dates

First Submitted

June 1, 2025

First Posted

June 10, 2025

Study Start

September 19, 2024

Primary Completion (Estimated)

September 19, 2027

Study Completion (Estimated)

September 19, 2027

Last Updated

June 12, 2025

Record last verified: 2025-06

Data Sharing

IPD Sharing
Will not share

Locations