Orogastric Tube Insertion Clinical Trial
Official title:
The Effect of White Noise and Swaddling Methods in Reducing the Pain Caused by Orogastric Tube Insertion in Preterm Infants: A Randomized Controlled Trial
Verified date | January 2022 |
Source | Afyonkarahisar Health Sciences University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study is a randomized controlled experimental study designed to examine the effect of white noise and swaddling methods in reducing the pain caused by orogastric tube insertion in preterm infants. This study is planned to be conducted with 4 groups, consisting of 3 experimental groups and 1 control group. White noise, swaddling method, and white noise + swaddling methods will be the interventions during the study together with the standard care and procedures for the experimental groups, while the control group will only have standard care and procedures during the study.
Status | Active, not recruiting |
Enrollment | 132 |
Est. completion date | October 15, 2022 |
Est. primary completion date | May 1, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility | Inclusion Criteria: - With 32-34 weeks of gestation, - With the postnatal age between 3-28 days, - Birth weight is above 1000 grams, - With the Apgar score =7 at 1st and 5th minutes, - With stable vital signs, - Without any congenital anomaly, - Not receiving mechanical ventilator support and having spontaneous breathing, - Requested by the physician to place an orogastric tube and fed with an orogastric tube, - Breastfeeding (through an orogastric tube), - Not experienced a painful procedure at least half an hour before the interventions, - Without the use of opioid or non-opioid analgesic in their treatment, - Without congenital or acquired malformation related to hearing, - With parents written consent for the participation of their baby. Exclusion Criteria: - With the postnatal age outside 3-28 days, - Birth weight is = 1000 grams, - With the Apgar score <7 at 1st and 5th minutes, - With unstable vital signs, - With congenital anomaly in the face or the oral cavity, - Being on mechanical ventilator support, - With a congenital malformation that may affect respiration and cause asphyxia, - With intracranial bleeding or risk of bleeding, - With disorders affecting the cerebral circulation or cardiovascular system, - Subjected to a painful procedure at least half an hour before the interventions, - With opioid or non-opioid analgesic in their treatment, - With the surgical history, - With continuous sedative treatment, - With congenital or acquired malformation related to hearing, - Not being fed with an orogastric tube, - With parent not giving consent for the participation of their baby |
Country | Name | City | State |
---|---|---|---|
Turkey | Usak Öztan Hospital Neonatal Intensive Care Unit | Usak |
Lead Sponsor | Collaborator |
---|---|
Afyonkarahisar Health Sciences University |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The Premature Infant Pain Profile-Revised (PIPP-R) Change | The PIPP-R scale includes 3 behavioral (brow bulge, eye squeeze, nasolabial-furrow), 2 physiological (heart rate and oxygen saturation) and 2 contextual (behavioral state and gestational age) items. Each item has a score from 0-3. The highest score that can be obtained from the PIPP-R scale for preterm infants is 21.The mean scores obtained from the PIPP-R scale reflects mild level of pain as mild if it is between 0-6 points, moderate if it is between 7-12 points and severe if it is between 13-21 points. | 5 minutes, 3 minutes and 1 minute before the procedure. During the procedure. 1 minute, 3 minutes and 5 minutes after the procedure |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT06222047 -
Pain and Comfort Level During Orogastric Catheter Insertion in Preterms
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N/A |