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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03448432
Other study ID # PREGAN (29BRC17.0155)
Secondary ID
Status Recruiting
Phase N/A
First received February 22, 2018
Last updated March 2, 2018
Start date February 27, 2018
Est. completion date December 27, 2019

Study information

Verified date February 2018
Source University Hospital, Brest
Contact Marie-Anne Couturier
Phone 0298223421
Email marie-anne.couturier@chu-brest.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Anemia during pregnancy occurs in 41% of women. The most common etiology is iron deficiency, but studies to determine prevalence of other causes of anemia in pregnancy are still lacking. However, anemia in pregnancy lead to adverse pregnancy outcomes and increase risk of maternal and fœtal morbidity and mortality. Specific management of anemia is so needed.


Recruitment information / eligibility

Status Recruiting
Enrollment 700
Est. completion date December 27, 2019
Est. primary completion date October 27, 2019
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- woman 18-years or older

- woman with a normal pregnancy

- anemia with accidental or symptomatic discovery, whatever the term of pregnancy

- non opposition collected

Exclusion Criteria:

- Refuse to participate

- Stopped pregnancy whatever the term

- Medical abortion of pregnancy

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France CHRU de Brest Brest

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Brest

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prevalence of the etiologies of anemias occured during pregnancy Anemia in pregnancy is defined as hemoglobin level (Hb) < 11 g/dL in the first and the third trimesters, and Hb < 10.5 g/dL in the second trimester. from date of inclusion until 6 weeks after delivery
Secondary Study of obstetrical complications in women with anemia Measure of the incidence of postpartum haemorrhage, instrumental extractions, caesareans sections, premature delivery, intra-uterine growth restriction or small for gestational age, placenta abruption, preeclampsia and low birth-weight newborn (<3rd and <10th percentile under neonatal morphometry curves)
Level of release,
1-, 3- and 5-minutes Apgar score,
Arterial ans venous cord potential hydrogen (pH)
from date of inclusion until delivery
Secondary Study of the evolution of anemia during pregnancy and postpartum Measure of the Hb level monthly and at 6 weeks after delivery from date of inclusion until 6 weeks after delivery
Secondary Describe the etiological and therapeutic management of pregnancy anemias therapeutic management : etiologic treatment (supplemental iron, vitaminic replacement, others) and symptomatic treatment (numbers and rhythm of transfusions) from date of inclusion until 6 weeks after delivery
See also
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Not yet recruiting NCT06061393 - Comparison Between Outcomes of Pregnant Women Treated With Ferinject vs. Venofer for Iron Deficiency Anemia Phase 4
Recruiting NCT05975125 - The Effect of Vitamin C for Iron Supplementation During Pregnancy With Risk of Anemia N/A
Active, not recruiting NCT05739097 - Prospective Study on Feto-maternal outcoMe In aNemIc womEn
Enrolling by invitation NCT04810546 - Feasibility or Oral Lactoferrin to Prevent Iron Deficiency Anemia in Obese Pregnancy N/A
Withdrawn NCT03873571 - Adherence of Iron Succinylate Therapy in Pregnancy
Completed NCT04517734 - Erythroferrone and Its Impact on Maternal and Neonatal Iron Homeostasis
Recruiting NCT06434870 - Effect of Spinal Anesthesia in Elective Cesarean Cases on Frontal QRS Angle in Anemic and Non-Anemic Patients
Completed NCT04812821 - Statement of Care of Anemia in Delivering Patients at Nord Franche-Comte Hospital