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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 2 March 2015
Main ID:  NCT02363569
Date of registration: 02/02/2015
Prospective Registration: No
Primary sponsor: Meir Medical Center
Public title: The Prognosis of Early Pregnancy With Post Coital Bleeding
Scientific title: The Prognosis of Early Pregnancy With Post Coital Bleeding Compared to Early Pregnancy With Spontaneous Bleeding
Date of first enrolment: February 2015
Target sample size: 120
Recruitment status: Not yet recruiting
URL:  http://clinicaltrials.gov/show/NCT02363569
Study type:  Observational [Patient Registry]
Study design:  Observational Model: Cohort, Time Perspective: Prospective  
Phase:  N/A
Countries of recruitment
Israel
Contacts
Name:     Meir Pomeranz, M.D
Address: 
Telephone:
Email:
Affiliation:  Meir Hospital, Israel
Name:     Meir Pomeranz, M.D
Address: 
Telephone: +972537482770
Email: Pomeranzmiki@clalit.org.il
Affiliation: 
Key inclusion & exclusion criteria

Inclusion Criteria:

- women (age 18-40) with early pregnancy (4-23 weeks) with singleton or twins
pregnancy that address to the "Women E.R." due to vaginal bleeding.

Exclusion Criteria:

- age >40 or <18

- women with history of more then 3 abortions.

- women with history of more then 2 pre term labor

- ectopic pregnancy

- placental previa

- women who takes anticoagulation therapy

- women with known pathology at cervix.

- women with known uterus defect. pregnancies with chromosomal defects or birth defects
that was discovered at the screening tests.



Age minimum: 18 Years
Age maximum: 40 Years
Gender: Female
Health Condition(s) or Problem(s) studied
Vaginal Bleeding During Pregnancy
Postcoital Bleeding
Intervention(s)
Primary Outcome(s)
Newborn Complications (low apgar, small gestational age , need for blood transfusion, artificial respiration, infection) [Time Frame: after they give birth (8 month after they address to the E.R.)]
Delivery Complications (cesarean section,assisted delivery) [Time Frame: after they give birth (8 month after they address to the E.R.)]
Pregnancy Complications (abortion, pre eclampsia, pre term labor,, cervix shortening, gestational diabetes, placental abruption, P-PROM(pre mature rupture of membrane), intrauterine growth retardation , Hypertension) [Time Frame: after they give birth (8 month after they address to the E.R.)]
Secondary Outcome(s)
Secondary ID(s)
MeirMc 180-12
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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