Trials / Not Yet Recruiting
Not Yet RecruitingNCT06684080
The Effectiveness of a Care Bundle to Prevent Postpartum Hemorrhage After Cesarean Delivery
A Cluster Randomized Trial on the Effectiveness of a Care Bundle to Prevent Postpartum Hemorrhage After Cesarean Delivery (Re-Team)
- Status
- Not Yet Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 52,000 (estimated)
- Sponsor
- Dunjin Chen · Academic / Other
- Sex
- Female
- Age
- —
- Healthy volunteers
- Not accepted
Summary
Delays in the detection or inconsistent use of effective interventions of postpartum hemorrhage can result in complications or death. We designed a cluster-randomized trial to assess a multi-component strategy for the detection and treatment of postpartum hemorrhage after cesarean delivery.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | A care bundle | 1. Risk evaluation for PPH and Reserve plan; 2. Assess blood loss using Estimated Blood Loss Form and amnion fluid collection drape; 3. Satisfy any of the following conditions: i. If the estimated blood loss reaches 500ml but is less than 1000ml, and any of the following abnormal indicators are present; ii. If the estimated blood loss reaches 1000ml, no other indicators need to be considered: 1) Lack of uterine contractions 2) Persistent bleeding 3)Shock index (heart rate/systolic blood pressure) was greater than 0.9 Initiate the following protocols①, ②, ③, ④ * Maintain uterus tone (Administration of Oxytocin and second-line medications to promote uterine contraction) * Intravenous infusion ③ Administered tranexamic acid ④ Multi-methods and Multi-disciplinary |
Timeline
- Start date
- 2025-01-01
- Primary completion
- 2026-12-31
- Completion
- 2027-06-30
- First posted
- 2024-11-12
- Last updated
- 2025-01-01
Source: ClinicalTrials.gov record NCT06684080. Inclusion in this directory is not an endorsement.