Status:

UNKNOWN

Postpartum Oxygen Inhalation for the Treatment of Postpartum Haemorrhage

Lead Sponsor:

Erzincan Military Hospital

Conditions:

Postpartum Hemorrhage

Eligibility:

FEMALE

20-40 years

Phase:

PHASE4

Brief Summary

In the aetiology of postpartum uterine atony, hypoxia is considered an important factor although some suggest that peripheral oxygen saturation is not influenced by oxygen inhalation in women during t...

Eligibility Criteria

Inclusion

  • gestational age between 37 and 42 weeks;
  • singleton pregnancy;
  • live fetus;
  • cephalic presentation;
  • neonatal birth weight of 2500-4500 g;
  • parity between one and five;
  • maternal age \< 35 years old;
  • vaginal birth

Exclusion

  • blood pressure ≥ 140/90mmHg;
  • placenta previa;
  • placental abruption;
  • a history of any bleeding during pregnancy;
  • a history of curettage;
  • cesarean section or any uterine scar;
  • a history of postpartum hemorrhage;
  • polyhydramnios;
  • signs or symptoms of maternal infection;
  • known uterine anomalies;
  • history of any drug use during labor;
  • abnormal placentation;
  • coagulation defects;
  • instrumental deliveries;
  • hemoglobin concentration \< 8 g/dL;
  • history of anticoagulant drugs;
  • beta-mimetic medications during pregnancy;
  • prolongation of the first stage of labor \> 15 hours

Key Trial Info

Start Date :

May 1 2010

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

September 1 2010

Estimated Enrollment :

450 Patients enrolled

Trial Details

Trial ID

NCT01180192

Start Date

May 1 2010

End Date

September 1 2010

Last Update

February 14 2011

Active Locations (1)

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1

Bakirkoy Women's and Children's Teaching Hospital

Istanbul, Turkey (Türkiye)