Comparing the analgesic effects of oral Glucose, sterile water, Acetaminophen and Breastfeeding mothers in reducing neonatal pain.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201205319916N1

Enrollment

128

Registered

2012-09-16

Start date

2012-04-20

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

rediuce pain. Other medical procedures as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure

Interventions

Intervention 1: Of 128 newborn in this study are examined, in the first group the .32 neonate from 1ml of oral glucose 50% of as analgesic substance will be used two minutes before the process and up

Treatment - Drugs

Of 128 newborn in this study are examined, in the first group the .32 neonate from 1ml of oral glucose 50% of as analgesic substance will be used two minutes before the process and up to 45 seconds la

Of 128 neonate in this study. 32 the neonates in the Group II will be examined. the breast milk of two minutes before the start of the process will be used and the neonate up to 45 seconds later foll

Of the 128neonate in this study. 32 the neonates in the third group, from oral acetaminophen 15 mg/kg/dose will be used two hours before the procedure and the noenates up to 45 seconds later will be

Of the 128 neonate in this study. 32 the neonates in Group IV, from 1ml sterile water two minutes, before the procedure will be used and to 45 seconds later, the neonate will be evaluated.

Eligibility

Sex/Gender

All

Age

1 Years to 28 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: all the term neonates and healthy with a weight of 2500 to 4000 grams admitted just because icter in hamedan hospitals and under the blood sampling. Exclusion criteria: anomalies at birth; asphyxia; prior painful intervention; circumcision, injection and admission for any cause other than jaundice.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: untle 45 second after intrvention. Method of measurement: covers scale.	—

Secondary

Measure	Time frame
Reduce of pain. Timepoint: 45 second. Method of measurement: covers scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZohreh Shalchi

Hamedan University of Medical Sciences

z.shalchi@umsha.ac.ir+98 81 1264 0044

Outcome results

None listed

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