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Effect of breast feeding and Sucrose on pain relief in neonates

Comparison survey between breast feeding and Sucrose on pain relief and physiological parameters during capillary sampling in neonates: A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014101919589N1
Enrollment
95
Registered
2014-12-12
Start date
2014-12-22
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

Acute pain. pain, not elsewhere classified

Interventions

Intervention 1: 2 ml of sterile water as placebo will be prepared and syringed in anterior part of the tongue 2 minutes before sampling. Intervention 2: 2 ml sucrose 25% will be prepared in advance an
Placebo
Treatment - Other
2 ml of sterile water as placebo will be prepared and syringed in anterior part of the tongue 2 minutes before sampling
2 ml sucrose 25% will be prepared in advance and syringed in anterior part of tongue 2 minutes before sampling
Infants will be breastfed in kangaroo care. Breastfeeding will be started 2 minutes before sampling and continue during the sampling. Infants are dressed, thus there is no skin to skin contact with mo

Sponsors

Vice-chancellor for research- Mashhad University of Medical Sciences, Mashhad, Iran
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Days to 5 Days

Inclusion criteria

Inclusion criteria: Inclusion criteria: filling the written informed consent by both parents; born at gestational age of =37 weeks; aged >24 hours (between 1-5 days); has 5 minutes APGAR score of = 7 Exclusion criteria: Medically instable infants; those who had received sedatives or analgesics in the past 48 hours; infants who had received naloxone in the previous 24 hours; preterm and Low Birth Weight (LBW) infants; Those who had been fed in the past 30 minutes

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Heart rate. Timepoint: each minute until 3 minutes after sampling. Method of measurement: cardiac monitoring.;Blood pressure. Timepoint: each minute until 3 minutes after sampling. Method of measurement: cardiac monitoring.;Capillary oxygen saturation level. Timepoint: each minute until 3 minutes after sampling. Method of measurement: cardiac monitoring.;Pain alleviating. Timepoint: each minute until 3 minutes after sampling. Method of measurement: neonatal infants pain scale score (NIPS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactEmadodin Darchini-Maragheh

Ferdowsi university campus, College of medicine

darchinime861@mums.ac.ir+98 51 3800 2463

Outcome results

None listed

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