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The Effect of Time Window for Umbilical Cord Clamping During Cesareans on Offspring Hemoglobin and Maternal Blood Loss

NCT05492214 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 360

Last updated 2023-05-31

No results posted yet for this study

Summary

This is a randomized controlled trial, aiming to evaluate the effects of time window for umbilical cord clamping during cesarean section on the health outcomes of offspring hemoglobin，maternal blood loss，and children's growth and development. It will be conducted in Liuyang city and Huantai county of China, and the targeted sample size is 360 (180 in each site). All the eligible pregnant women will be randomly assigned to one of the four groups (three intervention groups and one control group), and their babies will be followed up to 18 months of age.

Conditions

  • Delayed Cord Clamping
  • Hemoglobin
  • Blood Loss

Interventions

PROCEDURE

Delayed cord clamping (30s)

The same as that stated in arm descriptions.

PROCEDURE

Delayed cord clamping (60s)

The same as that stated in arm descriptions.

PROCEDURE

Delayed cord clamping (90s)

The same as that stated in arm descriptions.

Sponsors & Collaborators

  • National Natural Science Foundation of China

    collaborator OTHER_GOV

  • Liuyang Maternal and Child Health Care Hospital

    collaborator UNKNOWN

  • Women and Children's Health Care Hospital of Huantai

    collaborator UNKNOWN

  • Peking University

    lead OTHER

Principal Investigators

  • Jianmeng Liu · Peking University

  • Hongtian Li · Peking University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-09-22
Primary Completion
2023-05-08
Completion
2024-12-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05492214 on ClinicalTrials.gov