Trials / Completed
CompletedNCT04220320
The Success of Labor Induction Based on a Modified BISHOP Score.
The Success of Labor Induction Based on a Modified BISHOP Score Compared to Classic BISHOP Score and Cervical Length in Transvaginal Sonography.
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 758 (actual)
- Sponsor
- Rambam Health Care Campus · Academic / Other
- Sex
- Female
- Age
- 18 Years – 45 Years
- Healthy volunteers
- —
Summary
Pregnant women at term will be divided randomly into 3 groups: 1. Gynecological evaluation based on classic BISHOP score. 2. Gynecological evaluation based on a modified BISHOP score. 3. Gynecological evaluation based on cervical length as measured by transvaginal sonography. After gynecological evaluation, women will undergo induction of labor based on obstetric evaluation according to the group they were part of.
Detailed description
Women presenting to the obstetric emergency room for follow-up for various obstetric/other medical conditions over 37 weeks' gestation that are candidates for labor induction will receive an explanation regarding the study and sign informed consent. The women will be divided randomly into 3 groups: 1. Gynecological evaluation based on classic BISHOP score. 2. Gynecological evaluation based on a modified BISHOP score. 3. Gynecological evaluation based on cervical length as measured by transvaginal sonography. After gynecological evaluation, women will undergo induction of labor based on obstetric evaluation according to the group they were part of.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIAGNOSTIC_TEST | Vaginal examination. | Cervical properties as evaluated by a vaginal examination. |
| DIAGNOSTIC_TEST | Transvaginal sonography. | Cervical length as evaluated by a transvaginal sonography. |
Timeline
- Start date
- 2020-03-01
- Primary completion
- 2021-04-30
- Completion
- 2022-10-01
- First posted
- 2020-01-07
- Last updated
- 2022-10-26
Locations
1 site across 1 country: Israel
Source: ClinicalTrials.gov record NCT04220320. Inclusion in this directory is not an endorsement.