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The efficacy and safety of non-pharmocological interventions on repeated procedural pain in preterm infants

The efficacy and safety of non-pharmocological interventions on repeated procedural pain in preterm infants

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900020768
Enrollment
Unknown
Registered
2019-01-19
Start date
2019-01-31
Completion date
Unknown
Last updated
2019-01-28

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

Conditions

Pain

Interventions

Group 1:developmental care
Group 2:routine care

Sponsors

Hai-xia Gao
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: (1) Gestational age 30-32 weeks; (2) Hospitalized for the first time within 72 h after birth; (3) Apgar score of greater than or equal to seven at five minutes.

Exclusion criteria

Exclusion criteria: (1) Required mechanical ventilation; (2) Nothing by mouth status for any reason; (3) Unable to hear; (4) Had congenital anomalies; (5) Born to substance-abusing mother; (6) Intraventricular hemorrhage (grade III/IV); (7) Had hyperglycemia; (8)used opioid or sedative medication during hospitalization.

Design outcomes

Primary

MeasureTime frame
painful response and score;Growth and development;—

Secondary

MeasureTime frame
Safety;—

Countries

China

Contacts

Public ContactHai-xia Gao

Nanjing University of Chinese Medicine

bpn456@163.com+86 15105198352

Outcome results

None listed

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