Gauze tamponade in the lower uterine segment combined with abdominal binding for the treatment of primary postpartum haemorrhage following vaginal delivery: A Randomized Controlled Trial

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2500110990

Enrollment

Unknown

Registered

2025-10-23

Start date

2025-10-31

Completion date

Unknown

Last updated

2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postpartum hemorrhage

Interventions

Observation group:Place the tagged gauze into the lower uterine segment

Control group:According to standard management protocols for postpartum hemorrhage

Eligibility

Sex/Gender

Female

Age

18 Years to 45 Years

Inclusion criteria

Inclusion criteria: (1) Age: Female patients aged 18-45 years; (2) Full-term singleton pregnancy; hospitalized in our institution and delivered successfully, with immediate postpartum blood loss of 500 mL or more; (3) Participants voluntarily join this study, sign the informed consent form, have good compliance, and cooperate with follow-up.

Exclusion criteria

Exclusion criteria: (1) Twin pregnancy; (2) Dystocia (forceps or vacuum-assisted delivery), cesarean section, etc.; (3) Severe pregnancy complications or comorbidities; (4) Patients deemed ineligible by the investigator.

Design outcomes

Primary

Measure	Time frame
Blood loss in the first 2 hours after delivery;	—

Countries

China

Contacts

Public ContactHongjun Ying; Xiaobo He

Affiliated Women and Children's Hospital of Ningbo University, Ningbo, China.

hexiaobotj@163.com+86 83887067

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026