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Blood Components Changes by Using of Ringer's Lactated as Detergent In Autologous Blood Cell Transfusion

Blood Components Changes by Using of Ringer's Lactated as Detergent In Autologous Blood Cell Transfusion: A Prospective, Single-center, Open, and Single-arm Clinical Trial

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04927988
Enrollment
0
Registered
2021-06-16
Start date
2021-10-31
Completion date
2022-12-31
Last updated
2023-04-25

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

Conditions

Placenta Accreta Spectrum

Keywords

Placenta Accreta Spectrum, Autologous Blood Cell Transfusion, Blood Components

Brief summary

Placenta accreta spectrum (PAS) disorders are associated with increased maternal morbidity and mortality related to life-threatening hemorrhage, and greater potential need for blood transfusion. Clinical evidences have confirmed that the use of autologous blood cell transfusion is safe and effective for patients with obstetric haemorrhage. Normal saline is the solution recommended for red cell washing, administration and salvage. However, there is growing concern that normal saline is more toxic than balanced, buffered crystalloids such as Lactated Ringer's and Plasma-Lyte. The purpose of this study is to evaluate the blood components using of Ringer's Lactated by a prospective, single-center, open, and single-arm clinical trial.

Interventions

OTHERRinger's Lactated

Using of Ringer's Lactated In Autologous Blood Cell Transfusion

Sponsors

Maternal and Child Health Hospital of Foshan
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* Between 18 and 45 years old * Without health problem nor disease requiring regular medical treatment

Exclusion criteria

* subject with contraindication for drawing blood * Subject with physical or mental disability or restriction of liberty that would prevent autotransfusion

Design outcomes

Primary

MeasureTime frameDescription
Change in hematological parametersBaseline (Day 1), until 2 days after autotransfusionerythrocytes (/µL)

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026