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The Prognosis of Early Pregnancy With Post Coital Bleeding

NCT02363569 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 120

Last updated 2015-02-16

No results posted yet for this study

Summary

This is a prospective study, where the investigators will monitor pregnant women at 4-23 weeks of pregnancy coming to the "Women- E.R." at "Meir" Hospital due to spontaneous -or after intercourse- bleeding or bleeding secretions. The women will fill out questionnaires regarding past illness, vaginal bleeding, and gynecologic history. Then they will undergo full examination including ultrasound. After discharge, the investigators will recommend to all the women who came due to bleeding or bleeding secretions to avoid intercourse for two weeks after the bleeding stops. Afterwards they will be monitored until their delivery date (filling questionnaires a month after coming to the E.R. and at the end of the pregnancy). After they give birth the investigators will assess the rate of pregnancy, obstetric and embryonic complications in each of the study groups.

Conditions

  • Vaginal Bleeding During Pregnancy
  • Postcoital Bleeding

Sponsors & Collaborators

  • Meir Medical Center

    lead OTHER

Principal Investigators

  • Meir Pomeranz, M.D · Meir Hospital, Israel

Eligibility

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

Timeline & Regulatory

Start
2015-02-28
Primary Completion
2015-12-31
Completion
2016-12-31

Countries

  • Israel

Study Locations

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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 NCT02363569 on ClinicalTrials.gov