24 % sucrose to reduce dressing wound pain in neonate and infant

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

TCTR

Registry ID

TCTR20180804003

Enrollment

Unknown

Registered

2018-08-04

Start date

2017-12-01

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

surgical wound dressing pain 24% oral sucrose&#44

Interventions

routine wound dressing with pacifier,24% oral sucrose 2 minute with pacifier before routine wound dressing

No Intervention No treatment,Experimental Drug

control group,sucrose group

Eligibility

Sex/Gender

All

Age

No minimum to 1 Years

Inclusion criteria

Inclusion criteria: Age below than 1 year who have surgical wound dressing

Exclusion criteria

Exclusion criteria: Post conceptual age less than 32 weeks Patient who receive post operative opioid infusion NEC Risk of aspiration Infected surgical wound

Design outcomes

Primary

Measure	Time frame
efficacy of oral sucrose to reduce wound dressing pain 30, 120 and 240 second Neonatal in fant pain scale (NIPS)	—

Secondary

Measure	Time frame
risk factor of wound dressing pain 120 second risk factor of wound dressing pain	—

Contacts

Public ContactSahatsa Mandee

Faculty of medicine Siriraj hospital

sahatsa2@hotmail.com66816223601

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026