Image

Clinical Characteristics and Prognosis of Acute Stroke in Pregnancy and Puerperium

Clinical Characteristics and Prognosis of Acute Stroke in Pregnancy and Puerperium

Recruiting
Female
Phase N/A

Powered by AI

Overview

The objectives of this study are: (1) to describe the detailed clinical characteristics and prognosis of ASPP patients in order to explore the risk factors of ASPP, and to compare the short-term and long-term functional recovery outcomes between them and their controls; (2) to evaluate the risk of recurrent stroke, particularly during subsequent pregnancies, in ASPP patients; (3) to assess the short-term and long-term outcomes of their offsprings and their future development status.

This study is divided into three parts. The first part is a case-control study to explore the risk factors of ASPP and the predictors of the prognosis of ASPP patients. The second part is a cohort study to evaluate the impact of ASPP on the risk of recurrent stroke. The third part is a cohort study to assess the impact of ASPP on the short-term and long-term outcomes of their offsprings by comparing the offsprings of ASPP patients with the offsprings of non-ASPP participants.

Eligibility

  1. Case-control Study and Cohort Study on Recurrent Stroke Risk:

Inclusion Criteria:

  1. Female patients ≥18 years of age;
  2. Patients or their legally acceptable representatives or relatives agree to collect personal information for this study and sign an oral or online written informed consent.

Exclusion Criteria:

  1. Patients or their legally acceptable representatives or relatives refuse follow-up;
  2. Patients missing critical baseline demographic, clinical or neuroimaging data.
  3. Cohort Study on Offspring Outcomes:

Inclusion Criteria:

  1. Female patients ≥18 years of age;
  2. Patients in pregnancy or within 6 weeks postpartum;
  3. Patients or their legally acceptable representatives or relatives agree to collect personal information for this study and sign an oral or online written informed consent.

Exclusion Criteria:

  1. Patients or their legally acceptable representatives or relatives refuse follow-up;
  2. Patients missing critical baseline demographic, clinical or neuroimaging data;
  3. Patients whose offsprings have congenital malformation or inborn error of metabolism;
  4. Patients with complications which may affect cerebral blood flow supply, such as amniotic fluid embolism, in pregnancy;
  5. Patients whose family members other than the parents and siblings of their offsprings have a history of severe mental illness, such as mental retardation, autism and schizophrenia;
  6. Patients undergo acute myocardial infarction in pregnancy;
  7. Patients undergo non-spontaneous stroke events due to other causes, such as cerebral infarction or hemorrhage caused by surgery.

Study details
    Pregnancy-associated or Puerperium-associated Acute Stroke

NCT06527807

Beijing Tiantan Hospital

14 October 2025

Step 1 Get in touch with the nearest study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

  Other languages supported:

First name*
Last name*
Email*
Phone number*
Other language

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.