Vaginal Bleeding During Pregnancy Clinical Trial
Official title:
The Prognosis of Early Pregnancy With Post Coital Bleeding Compared to Early Pregnancy With Spontaneous Bleeding
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.
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 - bleeding secretions. The women will be divided in to two groups
1. Pregnant women (age 18-40) at 4-23 weeks of pregnancy with spontaneous bleeding or
bleeding secretions
2. Pregnant women (age 18-40) at 4-23 weeks of pregnancy that have appealed to the "Women
ER" 24 hours after bleeding or bleeding secretions due to intercourse.
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) The doctor that had examined the women,
will have to fill out questionnaires regarding the bleeding source, the time after
intercourse, how long after the intercourse the bleeding had appeared and which kind of
examination he had carried out.
A month after their appeal to the E.R. and after they give birth ,the investigators will
assess the rate of pregnancy, obstetric and embryonic complications in each of the study
groups, by phone.
;
Observational Model: Cohort, Time Perspective: Prospective
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT03632824 -
Tranexamic Acid in Pregnancies With Vaginal Bleeding
|
N/A |