Post Term Pregnancy Clinical Trial
Official title:
Anterior Uterocervical Angle for Latent Phase Duration in Post Term Pregnancies
NCT number | NCT04848701 |
Other study ID # | 20.11.31 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | June 1, 2020 |
Est. completion date | October 30, 2020 |
Verified date | April 2021 |
Source | Sanliurfa Mehmet Akif Inan Education and Research Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
To evaluate the performance of uterocervical angle (UCA) in the prediction of latent phase duration in post term pregnancies
Status | Completed |
Enrollment | 90 |
Est. completion date | October 30, 2020 |
Est. primary completion date | October 30, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 40 Years |
Eligibility | Inclusion Criteria: - Patients with singleton pregnancies - Post term pregnancies - Patients with vertex presentation, - Patients with intact membranes - Patients with no uterine contractions Exclusion Criteria: - women with BMI >30, - multiparity and multiple pregnancies, - patients with macrosomia (>4500 gr), - patients with major fetal congenital abnormality or fetal death and any contraindications to vaginal birth (e.g. active genital herpes), - patients with abnormal Pap smears, - patients with a history of previous cesarean section, myomectomy, hysteroscopic surgeries, dilatation and curettages, loop electrosurgical excision procedures, and cervical conization. |
Country | Name | City | State |
---|---|---|---|
Turkey | Nefise Nazli Yenigül | Bursa |
Lead Sponsor | Collaborator |
---|---|
Sanliurfa Mehmet Akif Inan Education and Research Hospital |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | prediction of latent phase duration by uterocervical angle in post term pregnancies | In patients diagnosed with late term pregnancy, the uterocervical angle and cervical length were measured by transvaginal ultrasound (TVUS) at the time of admission to the delivery room before labor induction. | 5 months | |
Secondary | the relative success of UCA in active phase and duration of labor prediction in post term pregnancies | 5 months | 5 months |
Status | Clinical Trial | Phase | |
---|---|---|---|
Enrolling by invitation |
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