Comparison of single or multiple phase administration of oral sucrose 24%

Comparison of single or three stage administration of oral sucrose drop 24% on reducing the pain of newborns admitted in the intensive care unit

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

IRCT

Registry ID

IRCT20090813002342N8

Enrollment

120

Registered

2018-09-12

Start date

2017-01-30

Completion date

Unknown

Last updated

2018-10-11

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

Conditions

Pain in critically ill neonates hospitalized at intensive care unit. Pain, not elsewhere classified

Interventions

Intervention 1: Intervention group1: Newborns who receive 24% sucrose through bolus dose in one step, two minutes before heel prick. Intervention 2: Intervention group 2:Newborns who receive 24% sucro

Eligibility

Sex/Gender

All

Age

1 Days to 28 Days

Inclusion criteria

Inclusion criteria: 1 to 28 day neonates who need blood sampling

Exclusion criteria

Exclusion criteria: Weight<800 g Neonates with mechanical ventilation Neonates with necrotizing entrocolitis Neonates born from mothers with uncontrolled diabetic Neonates born with congenital anomaly in face No feeding by mouth Neonate with unstable hemodynamic condition Neonate receives antiepleptics, opiates or sedative drugs

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: From the 30 seconds before the drug is started up to 60 seconds after it is consumed (except for the duration of the druguse). Method of measurement: video taping.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammadreza Rafati

Sari University of Medical Sciences

rafati293@yahoo.com+98 11 3354 3083

Outcome results

None listed

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