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Birth Rate in Conservative Monitoring of Pregnancy Beyond the Date of Birth.

Birth Rate in Conservative Monitoring of Pregnancy Beyond the Date of Birth.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02680093
Enrollment
200
Registered
2016-02-11
Start date
2016-02-29
Completion date
2018-01-31
Last updated
2016-02-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy, Prolonged

Brief summary

Pregnant Women beyond the date of birth. will be followed while coming to routine monitoring. physiological parameter of cervical length will be measured as the differential predictor to determine their due date. the cervical length will be measured as part of routine gynecologic examination to women who come for routine over due date follow up. additional medical data will be collected from the patient medical record.- demographic data, and all the routine prenatal medical care the women will receive up to the delivery.and delivery outcomes.

Detailed description

The clinical part of the study: the first visit of pregnancy monitoring is carried out at 40 full weeks. First visit to make sure the gestational age to receive full medical anamnesis , perform physical examination and vaginal and NST and BPP. Also, assess the clinical weight and when the need arises assessment of weight sonography. monitoring fetal movements . The women are ordered to return for routine check ups every 3 days. from - 41 full weeks the women should come every two days and 42 weeks should be referred for induction. In practice, the women offered induction at 41 weeks + 3 or 4 days.

Interventions

OTHERCervical length in pregnant women.

Pregnant Women beyond the date of birth. will be followed while coming to routine monitoring. physiological parameter of cervical length will be measured as the differential predictor to determine their due date. the cervical length will be measured as part of routine gynecologic examination to women who come for routine over due date follow up. additional medical data will be collected from the patient medical record.- demographic data, and all the routine prenatal medical care the women will receive up to the delivery.and delivery out comes.

Sponsors

Tel-Aviv Sourasky Medical Center
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

1. Age 18-50 . 2. Individual fetus 3. The dating of gestational age based on first- trimester ultrasonography or by last menstrual 4. Gestational age between 39 weeks and 0 days to 41 weeks and 6 days . 5. The pregnant women is not in pain ( VAS \<3 ) while signing on consent to participate. 6. Normal fetal monitoring measures and Sonar 7. Expectant mother is in active labor 8. Consent to participate

Exclusion criteria

1. Multi-pass Pregnancy 2. Without accurate dating of gestational age based on first- trimester ultrasonography or by last menstrual 3. Indicators for abnormal fetal monitoring and / or Sonar 4. Active labor 5. pain ( VAS \> = 3 ) 6. Expectant mother does not agree to participate or delivery if consent was given earlier

Design outcomes

Primary

MeasureTime frameDescription
Time interval between measurement of cervical length and delivery2 weeks.According to our local protocol post date surveillance is stated from 40+0 weeks of gestation. Each gravida undergoes vaginal examination using sonographic measurement of cervical length(in mm) using trans-vaginal sonar.

Secondary

MeasureTime frameDescription
Delivery with in 48 hours48 hours
Delivery with in 7 days7 days
Necessity of labor induction duo to post date2 weeksyes or no. documenting what kind of induction performed.

Contacts

Primary Contactyariv yogev, professor
yarivy@tlvmc.gov.il97236925603

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026