Evaluation of the effect of Erythropoietin on Antropometric results;Evaluation of the effect of Erythropoietin on Edema
Phase 4
Recruiting
- Conditions
- prematurity.
- Registration Number
- IRCT20160511027853N2
- Lead Sponsor
- Qazvin University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Premature birth with gestational age at birth less than 35 weeks
Birth weight less than 2000 grams
No illness (healthy babies who experience no problems or sickness in the first week of birth).
Exclusion Criteria
Congenital anomalies
depression
thrombocytopenia
diastolic pressure greater than 60 mmHg
shock
hydrops fetalis
threesomes
seizures
hemolytic diseases.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Around the head. Timepoint: Birth, one week after birth, two weeks after birth, forty days after birth. Method of measurement: Tape Measure.;Weight. Timepoint: Birth, one week after birth, two weeks after birth, forty days after birth. Method of measurement: Baby digital scale with SCEA brand, Model 374, which weighs 5 grams.;Edema. Timepoint: daily. Method of measurement: Pitting Edema Grading Scale.;Height. Timepoint: Birth day and forty day of birth. Method of measurement: Tape Measure.
- Secondary Outcome Measures
Name Time Method The general condition of the neonate. Timepoint: every hour. Method of measurement: General examination of infants in terms of tachypnea, cyanosis, lactation, excretion, weight gain.