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Supportive Status and Venipuncture Pain in Premature Infants

The Effect of Evolutionary Supportive Status on Pain Resulting from Venipuncture in Premature Infants Admitted to Neonatal Intensive Care Unit

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170813035662N2
Enrollment
56
Registered
2018-07-08
Start date
2017-02-12
Completion date
Unknown
Last updated
2018-09-11

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

Conditions

Premature Infants.

Interventions

Intervention 1: In the intervention group, that neonate put in evolutionary support status for 20 minutes that way the baby is in the latral or abdomen, the hands are bent and placed near the face and

Sponsors

Deputy of Research of Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Parental satisfaction Gestational age 28_36 Stability of hemodinamic status Lack of skeletal, muscular, neurological disorders

Exclusion criteria

Exclusion criteria: Lack of parental consent to continue cooperation in research Using sedative medicines Need for mechanical ventilation Need surgery

Design outcomes

Primary

MeasureTime frame
Facial Expression scale. Timepoint: Before the intervention begins, before kneading, simultaneously with the introduction of angiogist needle, 2 and 5 minutes after the needle is pulled out. Method of measurement: Neonatal facial coding system.;Respiratory rate. Timepoint: Before the intervention begins, before kneading, simultaneously with the introduction of angiogist needle, 2 and 5 minutes after the needle is pulled out. Method of measurement: Counting abdominal movements for one minute.;Heart rate. Timepoint: Before the intervention begins, before kneading, simultaneously with the introduction of angiogist needle, 2 and 5 minutes after the needle is pulled out. Method of measurement: Oxymetric pulse device.;Percentage of arterial oxygen saturation. Timepoint: Before the intervention begins, before kneading, simultaneously with the introduction of angiogist needle, 2 and 5 minutes after the needle is pulled out. Method of measurement: Oxymetric pulse device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Yazdanpanahi

Fatemeh School of Nursing and Midwifery Shiraz

stud2300992655@sums.ac.ir+98 933 171 4800

Outcome results

None listed

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