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Timing of Umbilical Cord Clamping in Preterm Neonates

Timing of Umbilical Cord Clamping in Preterm Neonates: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06000800
Enrollment
4
Registered
2023-08-21
Start date
2021-11-18
Completion date
2022-12-21
Last updated
2023-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cord Clamping

Keywords

Umbilical cord clamping, Preterm Neonates, Randomized Controlled Trial

Brief summary

Umbilical cord clamping is an important intervention that routinely done for all neonates afterbirth. yet the optimal timing for this intervention remains controversial

Detailed description

The study was a randomized controlled trial to assess the effect of timing of umbilical cord clamping on preterm neonatal outcome together The study was conducted in Kasr Al Ainy maternity hospital, Cairo university hospitals which provides free obstetrics and gynecology health services including antepartum, intraparturm, postpartum, and neonatal care for both low risk and high-risk pregnant women A total of 80 pregnant women out of 120 meeting the eligibility criteria were randomly pooled using computer-generated random numbers. The 80 randomly recruited ladies were randomly allocated using sealed envelopes to a group from 4 equal groups (group A, B, C, and D) of 20 ladies each. Umbilical cord clamping was performed immediately after birth (5 second) in group A, at 30 seconds in group B, at 60 seconds in group C, and at 90 seconds in group D.The trial was unblinded; where the participants and researchers were aware of the group a participant belonged to. After the study protocol was granted the ethical approval from the research ethical committee of Faculty of Nursing, Cairo University, Egypt, a written informed consent was obtained form mothers of preterm neonate who met the inclusion criteria including the aim, procedure, benefits, and nature of the study .The anonymity and confidentiality of information was assured, and the mothers had the right to withdraw from the study at any time during the study without any effect on the care provided to their preterm neonates. All study subjects were interviewed using a Structured interview questionnaire to obtain full history to assess participants' demographic data such as age, residence, educational level and occupation, past medical and surgical history, and obstetric history such as gravidity, parity, and current pregnancy antenatal care. Immediately after birth, neonates in all groups are held 20 cm below the incision level.For neonates in group A,umbilical cord was clamped and cut immediately after birth (5 second); while, neonates in group B, umbilical cord were clamped and cut at 30 seconds. For neonates in group C, umbilical cord was clamped and cut at 60 seconds. And finally, neonates in group D, umbilical cord were clamped and cut at 90 seconds. After cord clamping, all neonates were subject to routine immediate care. Neonatal data recorded included neonatal characteristic such as gestational age,birth weight and gender.Neonatal condition was assessed and documented immediately after birth through applying APGAR score of neonatal life, birth weight was measured immediately after delivery through birth scale. Vital signs (respiration, pulse & temperature) were measured birth. A pilot study was conducted on 10% of the study subjects. Eight preterm neonates who met the inclusion criteria; the pilot study was carried out to test the clarity of the tool's questions, and time needed to complete the tools. Additionally, to examine the applicability of the study tool, and to identify any difficulties that may arise and need to be handled before data collection. The pilot study revealed that the tools did not require modification. The sample included in the pilot study was excluded from the main study sample. The collected data will be coded and statistically analyzed to obtain mean and standard deviation for quantitative variables and frequencies (number of cases) and relative frequencies (percentages) for categorical variables. Comparisons between groups will bedone using analysis of variance (ANOVA) with multiple comparisons post hoc test in normally distributed quantitative variables while non-parametric Kruskal-Wallis test and Mann-Whitney test will be used for non-normally distributed quantitative variables . For comparing categorical data, Chi square test will be performed.

Interventions

OTHERGroup B

Umbilical cord clamping at 30 seconds

OTHERGroup C

Umbilical cord clamping at 60 seconds

OTHERGroup D

Umbilical cord clamping at 90 seconds

OTHERGroup A

Umbilical cord clamping immediately after birth (5 second)

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Masking description

The trial was unblinded; where the participants and researchers were aware of the group a participant belonged to

Intervention model description

A randomized controlled trial was used to fulfill the aim of the study. The randomized control trial (RCT) is a trial in which subjects are randomly assigned to one of two groups: one (the experimental group) receiving the intervention that is being tested, and the other (the comparison group or control group) receiving an alternative treatment

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

* healthy pregnant mothers * singleton fetuses * preterm cesarian delivery

Exclusion criteria

* asphyxiated neonates * twins * mothers with any medical or obstetrical conditions occurring intrapartum such as hemorrhage, or eclampsia.

Design outcomes

Primary

MeasureTime frameDescription
neonatal vital signs1st,6th,12th, 24th, and 48th hoursrespiration
neonatal hematocrit1st,6th,12th, 24th, and 48th hoursmeasuring this labs for neonate
neonatal bilirubin level test1st,6th,12th, 24th, and 48th hoursmeasuring this labs for neonate
neonatal APGAR score1st, 5th and 10th minutes of lifequick test performed at 1 and 5 minutes after birth to determine the physical condition of the newborn. The five categories assessed are heart rate, respiratory effort, muscle tone, reflex irritability, and color ( score from 8-10 means normal) score from 7-4 moderate asphyxia, from 1-3 sever asphyxia
neonatal hemoglobin1st,6th,12th, 24th, and 48th hoursmeasuring this labs for neonate

Secondary

MeasureTime frameDescription
oxygen saturation1st,6th,12th, 24th, and 48th hoursmeasuring this labs for neonate
blood glucose1st,6th,12th, 24th, and 48th hoursmeasuring this labs for neonate

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026