Status:
COMPLETED
Cervical Traction and Postpartum Hemorrhage
Lead Sponsor:
Ege University
Collaborating Sponsors:
The Scientific and Technological Research Council of Turkey
Conditions:
Postpartum Hemorrhage
Eligibility:
FEMALE
19-40 years
Phase:
NA
Brief Summary
The purpose of the research conducted within the scope of the doctoral thesis study is to evaluate the effect of cervical traction applied at the end of the third stage of childbirth on the oxytocin l...
Detailed Description
The research is a randomized controlled intervention study planned to evaluate the effect of the cervical traction maneuver applied at the end of the third stage of labor on oxytocin level and postpar...
Eligibility Criteria
Inclusion
- Pregnant women aged 18 and over who are not of advanced age
- Non-risky pregnancies (pregnant women without systemic disease, without placental problems such as placenta previa, without fetal problems (eg: low birth weight, intrauterine growth retardation, macrosomia, presentation disorders), those without obstetric problems
- Pregnant women who do not have pre-existing maternal hemorrhagic disorders such as factor 8 or 9 deficiency or VonWillebrand disease,
- Pregnant women with hemoglobin level HB \<10 mg / dl and without previous C/S)
- Pregnant women with live fetuses
- Pregnant women at term (those who are older than the 37th week of pregnancy and less than the 42nd week of pregnancy)
- Those who can speak Turkish
- Pregnant women who gave consent to participate in the study were included.
Exclusion
- It may occur in the first stage of labor; Pregnant women with pathological conditions such as non-progressive labor, abruption of the placenta, rupture, bleeding, cord prolapse, fetal distress, shoulder impingement,
- Pregnant women who have undergone induction of labor (induction with prostaglandin),
- It may occur in the second stage of birth; Pregnant women with pathological conditions such as shoulder insertion, bleeding and prolongation in the second stage, fetal distess, difficult delivery, vacuum and forceps application,
- It may occur in the third stage of birth; bleeding, placental retention, cavity control, third and fourth degree tear, etc. Pregnant women in situations such as
Key Trial Info
Start Date :
November 1 2022
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 30 2023
Estimated Enrollment :
200 Patients enrolled
Trial Details
Trial ID
NCT06179147
Start Date
November 1 2022
End Date
June 30 2023
Last Update
December 21 2023
Active Locations (1)
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1
Ege University Faculty of Health Sciences
Karşiyaka, İ̇zmi̇r, Turkey (Türkiye), 35575