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Effect of pacifier in preterm infant

Clinical Trial of Effect of Pacifier on physiologic criteria and feeding tolerance in preterm infant According to the NHS(national health system) Guideline of NNS.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016060628295N1
Enrollment
76
Registered
2017-01-28
Start date
2016-01-21
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

Feeding tolerance and physiologic criteria in preterm infants. Disorders related to short gestation and low birth weight, not elsewhere classified

Interventions

Intervention 1: infants in intervention group recieved pacifier according to the NNS guidline 10 minute before feeding,during and after feeding until the infant wants to suck the pacifier.The pacifier
infants in intervention group recieved pacifier according to the NNS guidline 10 minute before feeding,during and after feeding until the infant wants to suck the pacifier.The pacifier was used in thi
Control group:infants in control group just take routine care and didn't received pacifier.every 6 hour,we filled the checklist for them.

Sponsors

Vice Chancellor For Research, Mashhad University Of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 31 Days

Inclusion criteria

Inclusion criteria: Inclusion criteria: Gestational age between 26 to 32 weeks according to the Ballard scale; Age of birth up to 48 hours; birth weight less than 1500 g; no previous feeding (Along with the study, tube feeding for the infant begins); Lack of respiratory distress requiring intubation and ventilator; Lack of asphyxia; Lack of mother addiction; Having first and the fifth minute Apgar score above 7; No anomaly of the jaw, mouth and gastrointestinal tract like cleft lip, cleft palate and Esophageal atresia. Exclusion criteria: Feeding intolerance and NPO during the study; The need for intubation during study; The incidence of NEC during the study; Intraventricular hemorrhage (grade 3 and 4); Hospital Stay less than 7 days; Sepsis during the study; The reluctance of parents to continue to participate in the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Physiologic criteria including Heart rate, respiratory rate and o2 saturation. Timepoint: every 6 Hour. Method of measurement: with pulse oxymetery and counting respiratory rate.;Feeding tolerance including vomiting, residue,abdominal distension and defecation. Timepoint: every 6 Hour(6,12,18,24). Method of measurement: Observation and complete the checklist.

Secondary

MeasureTime frame
_. Timepoint: _. Method of measurement: _.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParisa Rahnama

Mashhad university of medical science

rahnamap2@mums.ac.ir+98 51 3859 1511

Outcome results

None listed

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