Clinical Trials Logo

Clinical Trial Summary

The aim of this study is to assess the values of MCA PI / UA PI and MCA RI / UA RI ratios and amniotic fluid volume in predicting the adverse perinatal fetal outcome in uncomplicated postdate pregnancy


Clinical Trial Description

The Study Will be a case-control study that will be conducted at Banha University Hospital and AFHSR in Saudi Arabia after the approval of Institutional ethical committee. One hundred pregnant women will be recruited from antenatal clinic. Starting from November 2022. An informed consent will be obtained from the patients . The patients will be subdivided into two groups: Group 1(Control Group):consist of 100 pregnant females with gestational age 37-40 weeks. Group 2 (post date Group):consist of 100 pregnant females with gestational age 41 weeks or more. Inclusion criteria: 1. Singleton, viable fetus in the vertex presentation. 2. History of regular menstrual cycles. 3. Gestational age calculated from the first day of last menstryal period or by first-trimester or second-trimester (before 20 weeks) ultrasound examination. 4. No obstetric or medical complications of pregnancy apart from post-date pregnancy All patients will be subjected to: 1. Detailed history: including, personal history, menstural history, obstetric history, present history and past history. 2. Physical examination: general, abdominal and pelvic examination. 3. Investigations: including, A- Ultrasound examintion for amniotic fluid index (AFI) measurement. B- Doppler studies: i - Middle cerebral artery pulsatility index (MCA -PI) and resistace index(MCA-RI). ii - Umbilical artery pulsatility index (UA-PI) and resistance index (UA-RI). iii - Cerebro-Placental ratio (CPR). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02255903
Study type Observational
Source Benha University
Contact khalid Ibrahim, MD
Phone 201281469651
Email dr.khalidkhader77@yahoo.com
Status Recruiting
Phase
Start date February 2022
Completion date August 2023

See also
  Status Clinical Trial Phase
Completed NCT01542151 - Effects of Sleep, Fatigue, and Timing of Post-dates Inductions Among Nulliparas N/A
Completed NCT02916082 - Cervical Length Pre-induction as a Tool to Predict Vaginal Birth N/A
Recruiting NCT03607929 - HIDRATA Study: Efficacy of a Hydration Protocol in Nulliparous Women During Labor N/A
Not yet recruiting NCT04307199 - Membrane Sweeping to Prevent Post-term Pregnancy: The MILO Study N/A
Terminated NCT04299438 - Propranolol Rescue of Prolonged Labor Phase 3
Completed NCT01140971 - Foley Catheter Versus Vaginal Misoprostol for Cervical Ripening and Induction of Labor N/A
Not yet recruiting NCT02680093 - Birth Rate in Conservative Monitoring of Pregnancy Beyond the Date of Birth. N/A