Status:
COMPLETED
Evaluation the Blood Loss in Pregnancies With Misoprostol-induced Labour
Lead Sponsor:
Maternidade Escola Assis Chateaubriand
Conditions:
Pregnancy
Induced Labor
Eligibility:
FEMALE
14-40 years
Phase:
PHASE4
Brief Summary
The purpose of this study is to evaluate the blood loss in induced vaginal delivery by misoprostol and caesarians section with induction attempt.
Detailed Description
Methods: it was a study achieved with 101 pregnant women with indication to induced delivery labor that were evaluated by the hemoglobin dosage pre and post delivery for estimate the blood loss at del...
Eligibility Criteria
Inclusion
- Indication of early elective delivery by induction of labor (pre-eclampsia, HELLP syndrome, chronic hypertension, prolonged gestation, diabetes mellitus, gestational diabetes, heart disease, thyroid disease;
- pregnancy with living fetus;
- vertex cephalic presentation;
- estimated fetal weight by ultrasound \> 2500g and \<4000g;
- Amniotic fluid index (AFI)\> 5 cm, except in cases of premature rupture of membranes in which AFI \<5 cm would be allowed;
- cardiotocography (CTG) antepartum normal;
- Bishop Score less than or equal to 6;
- Determination of hemoglobin pre and post-partum.
Exclusion
- Prior Cesarean section;
- previous uterine scar by myomectomy;
- Fetal presentation anomalous;
- Evidence of fetal abnormal (CTG, Ultrasound or Doppler);
- Fetal growth restriction;
- Gestation multiple;
- genital bleeding;
- tumors, malformations and / or ulceration in the region vulvoperineal and birth canal;
- No determination of hemoglobin pre-and post-partum;
Key Trial Info
Start Date :
February 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2009
Estimated Enrollment :
161 Patients enrolled
Trial Details
Trial ID
NCT01231126
Start Date
February 1 2008
End Date
January 1 2009
Last Update
November 16 2010
Active Locations (1)
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1
Maternidade-Escola Assis Chateaubriand
Fortaleza, Ceará, Brazil, 60430-270