The use of cell salvage in women undergoing Cesarean section for Central placenta

Status

Active, not recruiting

Phases

Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR-OIC-16008810

Enrollment

Unknown

Registered

2016-07-09

Start date

2016-08-01

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

central placenta

Interventions

group cell salvage :cell salvage

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: patients with diagnosis invasive central placenta used MRI or ultrasound who undergoing CS elective or emergency

Exclusion criteria

Exclusion criteria: patients refused blood type with Rh- history of transfusion Hb less than 70g/L has enrolled other studies

Design outcomes

Primary

Measure	Time frame
volume of autologous blood transfusion;volume of allogenetic RBC;cost related transfusion;	—

Contacts

Public ContactLi Jian

Wenzhou People's Hospital

313591073@qq.com+86 13758431800

Outcome results

None listed

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