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RecruitingNCT06935422CPRUpdated Sep 5, 2025

Role of Cerebroplacental Ratio Discordance at 16-20 Weeks in Predicting Monochorionic Twin Pregnancies' Specific Complications

An observational study in Monochorionic Twins and Cerebroplacental Ratio, sponsored by Ain Shams Maternity Hospital. Recruiting at 1 site in Egypt. Open to female participants. Per ClinicalTrials.gov, last updated 2025-09-05.

Sponsored by Ain Shams Maternity Hospital · Observational

From the registry’s dates

  • Primary completion was expected by Aug 2026, 3 months ago, but the record still lists the study as recruiting.
  • Started Mar 2025; still recruiting 1 year 8 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
55
Sex
Female
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Study summary

The purpose of this study is to evaluate the predictive value of CPR discordance at 16-20 weeks in MCDA twin pregnancies in predicting monochorionic-specific complications such as TTTS, TAPS, sFGR and IUFD of one or both fetuses

Read the detailed description

Monochorionic (MC) twin pregnancies are at a higher risk of perinatal morbidity and mortality because of the risk of developing unique complications. These include twin to twin transfusion syndrome (TTTS), selective fetal growth restriction (sFGR) , twin anemia polycythemia sequence (TAPS) and intrauterine fetal death (IUFD) of one or both fetuses. Therefore, early identification of these conditions is warranted to plan proper perinatal surveillance and management to improve outcome.

Sparse studies have found that inter-twin differences in Doppler ultrasound may occur prior to meeting diagnostic criteria for TTTS, TAPS, sFGR or adverse perinatal outcomes.

This study will try to reveal the potential clinical predictive value of inter-twin cerebroplacental ratio (CPR) discordance in the surveillance of MC twin pregnancies.

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Conditions studied

  • Monochorionic Twins
  • Cerebroplacental Ratio

Keywords

  • Monochorionic twins
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In context

Lead sponsor

Ain Shams Maternity Hospital is the lead sponsor of 139 studies on the registry; 8 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Female
Sampling method
Non-probability sample

Study population

Monochorionic diamniotic twin pregnancies with discordant cerebroplacental ratio at 16-20 weeks of gestation presenting to Ain Shams University Maternity Hospital for antenatal care.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Aged 18 years or more and able to consent.
  • Monochorionic Diamniotic twin pregnancy.
  • Discordant inter-twin cerebroplacental ratio at 16-20 weeks of gestation.

Exclusion criteria

Exclusion Criteria:

  • Fetal structural malformations or chromosomal abnormalities in any of the twins as detected by anomaly scan antenatally or neonatal examination postnatally (chromosomal abnormalities and some congenital malformations can interfere with normal fetal growth).
  • Identified infectious etiologies detected during immediate postnatal examination or during pregnancy (fetal infections can cause FGR ,usually symmetric type particularly if they occur in early gestation).
  • Referral after development of Twin to twin transfusion syndrome, twin anemia polycythemia sequence or selective fetal growth restriction.
  • Single fetal demise at the time enrollment in the study.
  • Conjoint twins.
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
55 participants (estimated)
Patient registry
No

Interventions

  • DeviceUltrasound

    Measuring cerebroplacental ratio discordance in monochorionic twins at 16-20 Weeks of gestation

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What researchers measure

Primary outcomes

  1. Development of monochorionic specific complications

    Monochorionic specific complications include twin to twin transfusion syndrome, twin anemia polycythemia sequence and selective fetal growth restriction

    Time frame: From 16-20 weeks of gestation till delivery.

Secondary outcomes

  1. Occurrence of intrauterine fetal death or perinatal mortality of one or both fetuses

    Gestational age upon occurrence of IUFD with clarifying if complications occur in the surviving twin in case of single fetal demise. Time and reason of perinatal mortality for any of the fetuses Wil be recorded.

    Time frame: From 16-20 weeks of gestation till 7th day of life

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Study locations

1 of 1 sites recruiting
  • Ain shams maternity hospital
    Cairo, Egypt
    Recruiting
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References and documents

Publications

  • Jain A, Acharya V, Shettikeri A, Sahana R, Radhakrishnan P. Intertwin discordance in MCA-PI and CPR in the prediction of TTTS progression. 19th world congress in fetal medicine. Ultrasound Obstet Gynecol. 2022;1(1):5-9.
  • Conde-Agudelo A, Villar J, Kennedy SH, Papageorghiou AT. Predictive accuracy of cerebroplacental ratio for adverse perinatal and neurodevelopmental outcomes in suspected fetal growth restriction: systematic review and meta-analysis. Ultrasound Obstet Gynecol. 2018 Oct;52(4):430-441. doi: 10.1002/uog.19117. Epub 2018 Sep 5. PubMed 29920817 ↗
  • Albu AR, Anca AF, Horhoianu VV, Horhoianu IA. Predictive factors for intrauterine growth restriction. J Med Life. 2014 Jun 15;7(2):165-71. Epub 2014 Jun 25. PubMed 25408721 ↗

Individual participant data

Plan to share: Yes — Name and email address

Supporting information: Study protocol

Time frame: From 2025 till 2028

Access criteria: Any researcher, physician or university lecturer Access for full study content

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 5, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06935422
Responsible party
Muhammed Ali Hassan Ali (Director, Ain Shams Maternity Hospital) — Principal investigator
First posted
Apr 20, 2025
Start date
Mar 1, 2025
Primary completion
Aug 1, 2026 (estimated)
Completion
Sep 15, 2026 (estimated)
Last update
Sep 5, 2025

Study contacts

Muhammed Ali Hassan, Assistant lecturer
Contact
muhammedali20191@yahoo.com
+201020256117
Mohamed Sameh Elswaify, Lecturer
Contact
+201285003060
Heba Abdelbaset Abd elkawy, Assistant professor
study chair · Ain Shams Maternity Hospital
Haitham Mohsen Elsabaa, Professor
study chair · Ain Shams Maternity Hospital
Amr Fathy Abd elkareem, Professor
study director · Ain Shams Maternity Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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