Effect of Maternal Hemoglobin on Neurobehavioural Development of Late Preterm Neonates : A Cohort Study
NCT ID: NCT02840292
Last Updated: 2016-07-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
100 participants
OBSERVATIONAL
2014-06-30
2014-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Developmentally Supportive Care on Neurobehavioral Outcome of Preterm Very Low Birth Weight Neonates
NCT02817022
Linear Growth and Neurobehavioural Outcome in PT Neonates (<34 Wks) at 37 and 40 Wks of CGA
NCT02970994
Brief Delay in Cord Clamping and Neurobehaviour in Preterms
NCT01753843
Effect of Infant Placement on Iron Stores in Infancy: A Pilot Study
NCT00675337
Anemia of Prematurity and Hemodynamics
NCT05496400
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Objective - To evaluate the neurobehavioral development at 37weeks of post conceptional age in late preterm infants born to mothers with hemoglobin \<11gm/dl; by a standardised scale - Neurobehavioral Assessment of Preterm Infants (NAPI).
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Cases
Late preterm neonates (\>34weeks but \<37weeks of gestation) with maternal hemoglobin \< 11gm/dl
No interventions assigned to this group
Controls
Late preterm neonates (\>34weeks but \<37weeks of gestation) with maternal haemoglobin ≥ 11gm/dl
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Clinically stable from respiratory, hemodynamic and metabolic point of view
* After receiving full, free, voluntary, informed consent from parents/family members within 24 hours of delivery.
Exclusion Criteria
* Congenital malformations (antenatally diagnosed or evident on clinical examination)
* Neonates admitted to NICU
* Neonates requiring ventilator support
* Neonates with any neurological impairment (IVH etc)
* Neonates undergoing surgery
* Neonates with birth asphyxia
* Neonates with birth trauma
* Confirmed history of substance abuse in mother.
34 Weeks
37 Weeks
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Lady Hardinge Medical College
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
DR. VIKRAM DATTA
Professor,Department of Neonatology
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Dr. Vikram Datta, MD, DNB
Role: STUDY_CHAIR
Lady Hardinge Medical College
Dr. Sanya Chandna, MBBS
Role: PRINCIPAL_INVESTIGATOR
Lady Hardinge Medical College
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Lady Hardinge Medical College
New Delhi, National Capital Territory of Delhi, India
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Hemoglobin and Neurobehaviour
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.