Effect of Birth on Immunological Parameters in Cord Blood

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

View full results

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-05-02

Study Completion Date

2017-10-12

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of the study is to understand the immediate effect of birth on immunological parameters in vaginally born cord blood.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Neurodegeneration in Newborns After Anesthetics

NCT03064607

Neurodegeneration General Anesthesia

COMPLETED

Safety and Efficacy of Autologous Umbilical Cord Blood Mononuclear Cells Transfusion in Neonates

NCT03053076

Safety Issues Effect of Drugs Neonatal Death

UNKNOWN PHASE1

New Procedure to Reduce Mother-newborn Separation

NCT06594458

Neonatal Disease

RECRUITING NA

Oropharyngeal Administration of Colostrum to Extremely Low Gestational Age Newborns

NCT01536093

Extremely Low Gestational Age Newborn Premature Infant

COMPLETED PHASE2

Triple Dye Plus Alcohol Versus Triple Dye Alone for Newborn Umbilical Cord Care

NCT00127699

Umbilical Cord Infection

COMPLETED PHASE1

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The main purpose of the study is to understand the immediate effect of birth on immunological parameters in vaginally born cord blood and also whether mode and duration of delivery has an influence on immune parameters in cord blood.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Immunologic Activity Alteration

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

This is not an interventional study

This is an observational study

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Pregnant mothers undergoing normal vaginal delivery

Exclusion Criteria

* Use of non-steroidal anti-inflammatory drugs (NSAIDs) 2 weeks prior to birth

* Antenatal antibiotics treatment (2 weeks prior to birth)
* Diabetes mellitus requiring insulin treatment during pregnancy
* Uncontrollable Hyperthyroidism during pregnancy

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes