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Search / Trial NCT06684080

The Effectiveness of a Care Bundle to Prevent Postpartum Hemorrhage After Cesarean Delivery

Launched by DUNJIN CHEN · Nov 11, 2024

Trial Information

Current as of July 22, 2025

Not yet recruiting

Keywords

Postpartum Hemorrhage Cesarean Delivery Randomized Trial Detection Treatment

ClinConnect Summary

This clinical trial is designed to study how effective a special care plan can be in preventing postpartum hemorrhage (excessive bleeding after childbirth) in women who have a cesarean delivery (a surgical procedure to deliver a baby). The trial will use a group of hospitals that have more than 100 cesarean deliveries each year to see if this comprehensive approach can help detect and treat bleeding more quickly and effectively, which could reduce complications and improve safety for mothers.

To participate in this trial, women must be having a cesarean delivery at a public hospital and be willing to sign a consent form that explains the study. However, if a hospital cannot provide certain data, or if a woman does not have blood test results from the two weeks before her surgery, she will not be eligible. While the trial is not yet recruiting participants, it aims to gather important information that could help improve care for mothers after cesarean deliveries in the future. If you or someone you know is interested, it’s a good idea to keep an eye out for when the trial starts.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Hospital level
  • 1. Public hospitals
  • 2. There are more than 100 cesarean deliveries per year
  • Patient level
  • 1. Cesarean delivery
  • 2. Sign informed consent
  • Exclusion Criteria:
  • Hospital level
  • 1. Data verification information cannot be provided
  • Pregnant woman level 1. No blood routine results within 2 weeks before surgery

About Dunjin Chen

Dunjin Chen is a dedicated clinical trial sponsor committed to advancing medical research through innovative studies and collaborative partnerships. With a focus on enhancing patient outcomes, Dunjin Chen leverages extensive expertise in trial design and regulatory compliance to facilitate the development of new therapies. The organization prioritizes ethical standards and patient safety while fostering a dynamic environment for scientific investigation. Through rigorous methodologies and a commitment to transparency, Dunjin Chen aims to contribute significantly to the healthcare landscape and improve the quality of life for patients worldwide.

Locations

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported