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Evaluation the Blood Loss in Pregnancies With Misoprostol-induced Labour

NCT01231126 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 161

Last updated 2010-11-16

No results posted yet for this study

Summary

The purpose of this study is to evaluate the blood loss in induced vaginal delivery by misoprostol and caesarians section with induction attempt.

Conditions

  • Pregnancy
  • Induced Labor

Interventions

DRUG

Misoprostol

Procedures were taken for induced labor delivery with misoprostol 25mcg, by vaginal rout. The pills were administered each 6 hours in a maximum number of six.

Sponsors & Collaborators

  • Maternidade Escola Assis Chateaubriand

    lead OTHER

Principal Investigators

  • Paulo César Praciano de Sousa, Mestre · Maternidade Escola Assis Chateaubriand

  • Francisco Edson de Lucena Feitosa, Doutor · Maternidade Escola Assis Chateaubriand

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
14 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-02-29
Primary Completion
2009-01-31
Completion
2009-01-31

Countries

  • Brazil

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01231126 on ClinicalTrials.gov