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Investigating the effect of fluid restriction on infants with transient tachypnea

Investigating the effect of fluid restriction on infants with transient tachypnea

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220806055625N3
Enrollment
120
Registered
2024-05-06
Start date
2023-12-22
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Transient neonatal tachycardia. Transient tachypnea of newborn

Interventions

Intervention 1: Intervention group: The number of 60 babies with respiratory distress in the intravenous fluid restriction group is 65 cc/Kg on the first day and a daily increase of 10 cc/Kg. Interven

Sponsors

Sanandaj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Days to 28 Days

Inclusion criteria

Inclusion criteria: Premature infants, post term, or term infants with tachypnea (respiratory rate greater than 60) may exhibit these characteristics. Infants who have transient radiological signs of tachypnea. Infants without radiological signs who have transient clinical symptoms of tachypnea and have been hospitalized within the first 6 hours after birth.

Exclusion criteria

Exclusion criteria: Infants who have congenital abnormalities. Infants who have other causes of respiratory distress, such as meconium aspiration syndrome, persistent pulmonary hypertension of the newborn, congenital diaphragmatic hernia, or surgical causes. Infants who are suspected of having sepsis. Infants who have asphyxia. Infants who are in shock. Infants who have a history of birth trauma. Infants who have positive blood culture. Infants who receive surfactant therapy during treatment.

Design outcomes

Primary

MeasureTime frame
Hospitalization days. Timepoint: upon discharge. Method of measurement: Refer to the patient's medical record.;Electrolyte and arterial blood gas levels. Timepoint: Upon arrival and 24 hours later. Method of measurement: It is performed on a blood sample taken from an artery or radial artery or other artery, and during it, the percentage of dissolved gases in the blood as well as the pH of the blood is calculated.;The respiratory distress level. Timepoint: Upon arrival and 24 hours later. Method of measurement: Observation and documentation by a trained NICU nurse.

Secondary

MeasureTime frame
Respiratory rate. Timepoint: upon admission and 24 hours later. Method of measurement: Documentation by a trained NICU nurse.;The level of respiratory support. Timepoint: upon admission and 24 hours later. Method of measurement: Documentation by a trained NICU nurse.;Weight gain. Timepoint: upon admission and 24 hours later. Method of measurement: The amount of weight gain measured with a digital scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSiros Hemmatpour

Sanandaj University of Medical Sciences

dr.siroshemmatour@yahoo.com+98 87 3362 7751

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026