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Efficacy of Controlled Therapeutic Hypothermia for Neonatal Hypoxic-Ischemic Encephalopathy (HIE)

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study aims to evaluate the effectiveness of therapeutic hypothermia in neonates diagnosed with hypoxic-ischemic encephalopathy (HIE). The study focuses on assessing both short-term outcomes after treatment and long-term neurological outcomes following therapeutic hypothermia.

Eligibility
Participation Requirements
Sex: All
Maximum Age: Newborn
Healthy Volunteers: f
View:

• Neonates diagnosed with hypoxic-ischemic encephalopathy (HIE) at the Neonatal Center, National Children's Hospital

• Gestational age ≥ 36 weeks

• Assessed using the modified Sarnat staging within the first 0-6 hours after birth

• Eligible for and/or treated with therapeutic hypothermia according to institutional protocol

• Underwent clinical and paraclinical monitoring during hospitalization

• Received brain magnetic resonance imaging (MRI) during the neonatal period (from 5 to 17 days of age)

• Availability of complete medical records for data collection and analysis

Locations
Other Locations
Viet Nam
Vietnam National Children's Hospitalv
RECRUITING
Ha Nội
Contact Information
Primary
DAT HUU TRAN
drtrandat1986@gmail.com
+84987836686
Time Frame
Start Date: 2025-06-10
Estimated Completion Date: 2028-02-01
Participants
Target number of participants: 120
Treatments
Experimental: Therapeutic Hypothermia
Neonates diagnosed with hypoxic-ischemic encephalopathy (HIE) who meet the protocol-defined eligibility criteria will receive therapeutic hypothermia. Eligible infants are those born at or after 36 weeks of gestation, younger than 6 hours of age, and meeting the required clinical and biochemical criteria for therapeutic hypothermia according to the study protocol.
Related Therapeutic Areas
Sponsors
Leads: National Children's Hospital, Vietnam

This content was sourced from clinicaltrials.gov

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