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?Effect of restrictive fluid management on the outcome of transient tachypnea of the newborn at ahvaz Imam Khomeini hospital

?Effect of restrictive fluid management on the outcome of transient tachypnea of the newborn at ahvaz Imam Khomeini hospital

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012111111432N1
Enrollment
82
Registered
2013-08-23
Start date
2012-08-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

transient tachypnea of the newborn. Respiratory distress of newborn

Interventions

Intervention 1: In the control group, in the first day of life 60ml/kg/d, in the second day 80ml/kg/d and from the third day 100 ml/kg/d of 10% dextrose water were administered. In cases who were care
Treatment - Other
In the control group, in the first day of life 60ml/kg/d, in the second day 80ml/kg/d and from the third day 100 ml/kg/d of 10% dextrose water were administered. In cases who were cared under radiant
In the intervention group, in the first day of life 40ml/kg/d, in the second day 60ml/kg/d and from the third day 80 ml/kg/d of 10% dextrose water were administered. In cases who were cared under radi

Sponsors

Ahvaz,Jundishapur University of Medical Siences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 1 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: neonate with in 34-0/7to 41-6/7 weeks age with: tachypnoea (RR>60) ;standing on tachypnea at least for 12 hrs; feature of CXR at least for one of these: prominent pulmonary hilus, increase thickness of lobar fisher due to accumulation of fluid, hilar congestion of both lung,flattening of diaphragm,increase AP diameter of chest exclusion criteria:neonate with congenital anomaly;systemic sepsis; mecunium aspiration; RDS; IUGR; fetal distress history; pneomonitis;congenital heart disease; DIC; multi organ failure; hypocalcemia; hypoglycemia; polycytemia; Na>150; Bun>20; K>5; Bill>15; urine out put<1cc/kg/hr

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Duration of oxygen requirement. Timepoint: during intervention. Method of measurement: hours.;Duration of CPAP requirement. Timepoint: during intervention. Method of measurement: hours.;Duration of VENTILATOR requirement. Timepoint: during intervention. Method of measurement: hours.;Hospitalized duration. Timepoint: during intervention. Method of measurement: days.

Secondary

MeasureTime frame
Urine out put. Timepoint: during intervention. Method of measurement: cc/kg/hr.;Serum BUN , CREATININ. Timepoint: during intervention. Method of measurement: serum sampling.;Serum K , Na. Timepoint: during intervention. Method of measurement: serum sampling.;Serum bilirubin. Timepoint: during intervention. Method of measurement: serum sampling.;Specific gravity of urine. Timepoint: during intervention. Method of measurement: with refractometer.;ABG. Timepoint: during intervention. Method of measurement: artery sampling.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasud Dehdashtian MD.

Ahvaz,JundishapurUniversity of medical Sciences

DEHDASHTIAN@aguns.ac.ir+98 61 1338 9669

Outcome results

None listed

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