Investigation and Comparing the effects of foot reflexology and sucrose 24% with pacifier on severity of neonatal Abstinence syndrome among the neonates with addicted mother

Investigation and Comparing the effects of foot reflexology and sucrose 24% with pacifier on severity of neonatal Abstinence syndrome, Hearth rate and Respiratory rate among the neonates with addicted mother

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20131228015965N20

Enrollment

Registered

2020-09-01

Start date

2019-10-22

Completion date

Unknown

Last updated

2020-09-07

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

Conditions

neonatal Abstinence syndrome. Neonatal withdrawal symptoms from maternal use of drugs of addiction

Interventions

Intervention 1: Intervention group 1: In the sucrose group with pacifier, 2 cc of sucrose solution for infants over 2 kg and 1.5 cc for infants 1.5 to 2 kg and 0.5 cc for infants under 1.5 kg of sucro

Eligibility

Sex/Gender

All

Age

1 Days to 28 Days

Inclusion criteria

Inclusion criteria: Newborns born with term maternal addiction during pregnancy Get a score of 8 or higher on the Finigan checklist Being hospitalized in educational and medical centers of the place of study Having parental consent

Exclusion criteria

Exclusion criteria: Having congenital problems, congenital anomalies and injuries during childbirth Having respiratory problems and other problems affecting the symptoms of deprivation

Design outcomes

Primary

Measure	Time frame
On severity of neonatal Abstinence syndrome. Timepoint: Twice a day for 12 hours, before and then 15 minutes and 2 hours after the intervention. Method of measurement: Fingan Tools.	—

Secondary

Measure	Time frame
Number of breaths. Timepoint: Twice a day 12 hours before the intervention, 15 minutes and 2 hours after the intervention. Method of measurement: Counting.;Heart rate. Timepoint: Twice a day 12 hours before the intervention, 15 minutes and 2 hours after the intervention. Method of measurement: Pulse oximetry device.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSedighe Gholami Shiri

Rafsanjan University of Medical Sciences

gholamidesigh@gmail.com+98 930 822 5514

Outcome results

None listed

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