Effectiveness of Oral 10% Glucose solution in reducing pain due to venipuncture in Infants 1month to 1 year

Comparison of the Effectiveness of Oral 10% Glucose solution with placebo in reducing pain due to venipuncture in Infants 1month to 1 year

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20140820018883N1

Enrollment

Registered

2018-02-21

Start date

2018-04-04

Completion date

Unknown

Last updated

2018-03-26

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

Conditions

Condition 1: Venipuncture ?acute pain in infants admitted to Emergency Department for acute diseases. Condition 2: Acute pain due to venipuncture.

Interventions

Intervention 1: Intervention group: Including Eligible infants between one month and one year old admitted to Emergency Department of Hospital. They will receive 2 milliliters 10% glucose solution, on

Eligibility

Sex/Gender

All

Age

1 Months to 1 Years

Inclusion criteria

Inclusion criteria: age:one month to one year old Need to indwelling catheter in Limb's'peripheral veins Candidate for Intravenous Fluid Therapy Informed consent of parents to participate the Infant

Exclusion criteria

Exclusion criteria: Disturbed of consciousness Life threatening conditions (poisoning,..)

Design outcomes

Primary

Measure	Time frame
Pain severity. Timepoint: two minutes before to two minutes after painful procedure (Venipuncture). Method of measurement: FLACC (Face, Legs, Activity, Cry, CONSOLability) scoring system.	—

Secondary

Measure	Time frame
Crying duration. Timepoint: from Intervention and two minute after that. Method of measurement: Observation and record by two independent observers.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHomeira Khoddam

Gorgan University of Medical Sciences

khoddam@goums.ac.ir+98 17 3245 6900

Outcome results

None listed

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