Effect of Delayed Cord Clamping in Preterm Neonates With Placental Insufficiency
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| ClinicalTrials.gov Identifier: NCT03731546 |
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Recruitment Status :
Completed
First Posted : November 6, 2018
Last Update Posted : June 16, 2020
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Preterm Infant Placental Insufficiency Placental Transfusion | Procedure: Delayed cord clamping | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 90 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Double (Participant, Outcomes Assessor) |
| Primary Purpose: | Supportive Care |
| Official Title: | Effect of Delayed Cord Clamping in Preterm Neonates With Placental Insufficiency |
| Actual Study Start Date : | December 1, 2017 |
| Actual Primary Completion Date : | December 30, 2018 |
| Actual Study Completion Date : | December 30, 2018 |
| Arm | Intervention/treatment |
|---|---|
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No Intervention: Group A
Placental insufficiency and ICC : Immediate cord clamping after delivery of the fetus in preterm infants with placental insufficiency
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Active Comparator: Group B
Placental insufficiency and DCC: Cord clamping 60 seconds after delivery of fetus in preterm infants with placental insufficiency
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Procedure: Delayed cord clamping
Cord clamping 60 seconds after delivery of fetus in preterm infants |
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Active Comparator: Group C
Normal placenta with DCC:Cord clamping 60 seconds after delivery of fetus in preterm infants without placental insufficiency
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Procedure: Delayed cord clamping
Cord clamping 60 seconds after delivery of fetus in preterm infants |
- Peripheral venous CD34 at admission [ Time Frame: first 24 hours of infants' life ]One milliliter of fetal blood will be taken from peripheral venous blood in the first 30 minutes of life and CD34 will be assessed by flow cytometry.
- Admission hemoglobin [ Time Frame: first 24 hours of infants' life ]One milliliter of neonatal blood will be taken from peripheral venous blood in the first 24 hours of life.
- Hemoglobin at 2 months [ Time Frame: 2 months of infants' life ]One milliliter of neonatal blood will be taken from peripheral venous blood at 2 months of life.
- Admission platelets [ Time Frame: first 24 hours of infants' life ]One milliliter of neonatal blood will be taken from peripheral venous blood in the first 24 hours of life.
- Admission WBCs [ Time Frame: first 24 hours of infants' life ]One milliliter of neonatal blood will be taken from peripheral venous blood in the first 24
- Phototherapy requirements [ Time Frame: first 28 days of life ]
- Polycythemia [ Time Frame: first 28 days of life ]
- Culture proven sepsis [ Time Frame: first 28 days of life ]
- Necrotizing enterocolitis [ Time Frame: first 28 days of life ]
- Intraventricular hemorrhage [ Time Frame: first 28 days of life ]
- Bronchopulmonary dysplasia [ Time Frame: first 70 days of life ]
- Need for nasal CPAP [ Time Frame: first 28 days of life ]
- Need for mechanical ventilation [ Time Frame: first 28 days of life ]
- Duration of oxygen therapy [ Time Frame: first 28 days of life ]
- Need for inotropes [ Time Frame: first 28 days of life ]
- Retinopathy of prematurity [ Time Frame: first 28 days of life ]
- Need for packed RBCs transfusion [ Time Frame: first 28 days of life ]
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| Ages Eligible for Study: | up to 1 Minute (Child) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- preterm neonates < 34 weeks gestational age
Exclusion Criteria:
- Vaginal bleeding due to placental abruption or tears Multiple pregnancies Suspected major fetal anomalies Suspected chromosomal aberration Maternal drug abuse Hydrops fetalis preterm who needed major resuscitative measures
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03731546
| Egypt | |
| Mansoura University Children's Hospital | |
| Mansourah, Egypt | |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Nehad Nasef, Professor of pediatrics/Neonatology, Mansoura University Children Hospital |
| ClinicalTrials.gov Identifier: | NCT03731546 |
| Other Study ID Numbers: |
MS/17.04.15 |
| First Posted: | November 6, 2018 Key Record Dates |
| Last Update Posted: | June 16, 2020 |
| Last Verified: | June 2020 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Delayed cord clamping Preterm Infant Placental Insufficiency Intrauterine growth restriction |
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Premature Birth Placental Insufficiency Obstetric Labor, Premature |
Obstetric Labor Complications Pregnancy Complications Placenta Diseases |

