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

T

Tel Aviv Sourasky Medical Center

Status

Unknown

Conditions

Pregnancy, Prolonged

Treatments

Other: Cervical length in pregnant women.

Study type

Observational

Funder types

Other

Identifiers

NCT02680093
0602-15

Details and patient eligibility

About

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.

Full 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.

Enrollment

200 estimated patients

Sex

Female

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

200 participants in 1 patient group

Cervical length in pregnant women.
Description:
Pregnant Women beyond the date of birth in conservative monitoring and prenatal follow-up. 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.
Treatment:
Other: Cervical length in pregnant women.

Trial contacts and locations

0

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Central trial contact

yariv yogev, professor

Data sourced from clinicaltrials.gov

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