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Predicting the Outcomes of Labor Induction

A

Ain Shams University

Status

Completed

Conditions

Induction of Labor Affected Fetus / Newborn

Treatments

Diagnostic Test: Manipal cervical scoring system

Study type

Observational

Funder types

Other

Identifiers

NCT03175406
ASU maternity hospital

Details and patient eligibility

About

Pre induction assessment using bishop scoring system and Manipal cervical scoring system performed on 105 pregnant females

Full description

preinduction cervical assessment using The Burnett modification of Bishop score with

  1. Cervical dilatation in centimeters will be given a score of zero if dilatation less than 1cm, a score of 1 if 1-2 cm dilated, a score of 2 if more than 2 cm dilataion.
  2. Length of the cervix will be given a score of zero if more than 2 cm, a score of 1 if 1-2 cm, a score of 2 if less than 1 cm.
  3. Station of fetal head will be given a score of zero if -2 or higher , a score of 1 if -1, a score of 2 if zero or lower.
  4. Consistency of the cervix will be given a score of zero if firm, a score of 1 if soft and a score of 2 if soft and stretchable.
  5. Position of the cervix will be given a score of zero if posterior, a score of 1 if mid position and a score of 2 if anterior. So, a total score (sum of all scores) of zero at a minimum to 10 at a maximum can be estimated.

and also preinduction cervical assessment using transvaginal ultrasound and Manipal system where:

  1. Length of the cervix will be given a score of zero if more than 3 cm, a score of 1 if 2-3 cm, a score of 2 if less than 2 cm.
  2. Length of the funnel will be given a score of zero if absent, a score of 1 if ≤ 0.5 cm, a score of 2 if more than 0.5 cm.
  3. width of the funnel will be given a score of zero if absent, a score of 1 if ≤ 0.5 cm, a score of 2 if more than 0.5 cm.
  4. cervical position and shape will be given a score of zero if curved, a score of 2 if straight
  5. Distance of presenting part to external os will be given a score of zero if more than 3 cm, a score of 1 if 2-3 cm, a score of 2 if less than 2 cm

Enrollment

105 patients

Sex

Female

Ages

20 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Singleton gestation at 37 completed weeks or greater .
  2. Cephalic presentation.
  3. Longitudinal lie.
  4. Living fetus.
  5. Intact membrane

Exclusion criteria

  1. Previous cesarean delivery or rupture uterus.
  2. Antepartum hemorrhage including (abruptio placenta, placenta previa or vasa previa).
  3. Abnormal fetal lie or presentation.
  4. Pervious uterine surgery as myomectomy.
  5. Category II, III non stress test.
  6. Pelvic structural deformity.
  7. Intrautrine growth retardation or macrosomia (estimated fetal weight ˃ than 4kg).
  8. Patients who received any pre induction ripening.
  9. Active genital herpes.
  10. Invasive cervical carcinoma

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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