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The comparsion early outcomes intermittent gavage in preterm infants

The comparsion early outcomes intermittent gavage in preterm infants :randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201408205168N7
Enrollment
96
Registered
2015-03-15
Start date
2015-04-04
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

Infant gavage outcome.

Interventions

Infant gavage with administered using a syringe in control group
Intervention 1: Infant gavage with gravity in intervention group. Intervention 2: Infant gavage with administered using a syringe in control group.
Prevention
Infant gavage with gravity in intervention group

Sponsors

Tabriz University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria:1- gastational age(28-34)week and AGA 2-NG tub feeding in sixth and seventh day 3-weight<2500gr 4- absence of major congenital malformation and heart disease 5- did not have any apnoea and shock in 24 hour 6-Disruption ventilation,NCPAP,HFNC 7-parents satisfaction 8-high apgar(fifth minuts apgar was more seven) 9- without umbilical vain catheter. Exclusion criteria:1- affection to PDA to need medical 2-NEC in execution time 3-sepsis 4-IVH(2 degree and more) 5-inexistence stability vital sign 6-lack of parents satisfaction 7-hypotention need to vasopresor

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Physiological index(heart rate,breathing and O2 saturation. Timepoint: Before ,execution time and 10 minuts after gavage in one day. Method of measurement: Before,execution time and 10 minuts after gavage written in check list.

Secondary

MeasureTime frame
Gastric residual volume is secondary outcom,emesis,abdominal distention and necrotizing enterocolits for two days checking instance side effect. Timepoint: Before feeding gavage every 2-3 hours in two days gastric residual checking and side effect recording in check list. Method of measurement: Aspiration of gastric contents from the indwelling nasal tube feeding every 2-3 hours and emesis with observation and abdominal distention and NEC with physician diagnosis.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahnaz Jabraeili

Tabriz University of Medical Science

jabraeilim@tbzmed.ac.ir+98 41 3477 0648

Outcome results

None listed

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