Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07012668

Outcomes and Risk Factors of Different Treatment Strategies for Neuro-co-cardiological Diseases and Post-cardiac Surgery Cerebrovascular Diseases

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.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Beijing Anzhen Hospital

Beijing, China

Location status: Recruiting

Location contact

Xin Tong, M.D.

CONTACT

[email protected]

17810651085 ext. 86

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

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

Treatment and study plan

Interventional or surgical treatment

Procedure

Simultaneous interventional or surgical treatment/staged interventional or surgical treatment

Primary outcomes

  1. Modified Rankin Scale Score

    Time frame: 90±7 days

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

Secondary outcomes

  1. Modified Rankin Scale Score

    Time frame: 7±1 days or the day discharged

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

  2. Modified Rankin Scale Score

    Time frame: 365±30 days

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

  3. Perioperative complication rate

    Time frame: 30±7 days

  4. Rate of cardiovascular and cerebrovascular events

    Time frame: 90±7 days

  5. Rate of cardiovascular and cerebrovascular events

    Time frame: 365±30 days

  6. Short-term complications

    Time frame: 90±7 days

  7. Long-term complications

    Time frame: 365±30 days

Study contacts

Contact information is provided by the study sponsor or research team.

Xiaochuan Huo, M.D.

CONTACT

[email protected]

+86 13716292262

Xin Tong, M.D.

CONTACT

[email protected]

+86 17810651085

Sponsors and collaborators

Lead sponsor

Beijing Anzhen Hospital

Other

Registry information

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Jun 10, 2025
Registry last updated
Jun 12, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.