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CompletedNCT05077345PAINUpdated Apr 7, 2022

The Effects of Different Procedures on Pain Levels at Preterm and Term Infants in Neonatal Intensive Care Unit

An observational study in Pain, Newborn and Preterm, sponsored by Sanko University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 1 Day to 8 Days. Per ClinicalTrials.gov, last updated 2022-04-07.

Sponsored by Sanko University · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
196
Ages
1 Day to 8 Days
Sex
All
01

Study summary

Accurate assessment of pain in neonates in the neonatal intensive care unit (NICU) is vital because of the high prevalence of painful experiences, including both daily procedural pain and postoperative pain, in this population. It has been reported that newborns born between the gestational ages (GY) 25-42 and hospitalized in the NICU undergo an average of 14 painful procedures per day in the first 2 weeks of life. The aim of this study is determinin the effect of different procedures on the pain levels of newborns in the Neonatal Intensive Care Unit (NICU).

Read the detailed description

Accurate assessment of pain in neonates in the neonatal intensive care unit (NICU) is vital because of the high prevalence of painful experiences, including both daily procedural pain and postoperative pain, in this population. Exposure of these infants to many mandatory invasive procedures and poor pain management during this time may lead to different results in the short and long term. Every painful application in newborns causes behavioral and physiological instability. Repeated exposure to painful stimuli produces long-term changes in stress-sensitive brain systems such as the hypothalamic-adrenal system and the developing brain. Therefore, evaluation and prevention of pain in newborns is essential. In the NICU, many medical interventions are often performed on infants that are repetitive, painful, but diagnostically necessary. All environmental stress factors can cause physiological changes such as increased pulse, blood pressure, respiratory rate and a decrease in oxygen saturation in newborns. Increasing energy expenditure to overcome these changes may affect physiological functioning, slowing recovery and adversely affecting the organization of the central nervous system (CNS). Heel blood (TC), vascular access (DY), naso and orogastric (NG-OG) catheter insertion, arterial blood collection, tracheal intubation (TE), various rectal procedures, removal of adhesive tapes, umbilical catheter (UK) insertion and removal, Various procedures such as aspiration, chest physiotherapy applications, diaper changing, various hand contacts, and general body care may induce pain responses in newborns. While these responses are associated with low cognitive and motor scores in early childhood, they may result in changes in visual-perceptual ability and somatosensory sensitivity later on. There are many studies in the literature to increase and prove the accuracy of pain assessment tools. However, since the pain treatments used in these studies were also varied, the homogeneity of the evaluations was insufficient. Therefore, more systematic evaluation studies should be conducted on how to improve pain management in NICUs. Finding which of the painful stimuli affects infants more will also guide the use of treatment methods. The aim of this study is to investigate the effects of different procedures applied in the NICU on the pain levels of term and preterm infants.

02

Conditions studied

  • Pain
  • Newborn
  • Preterm
  • Term
  • Venipuncture

Keywords

  • Newborn
  • pain
  • Preterm
  • Term
  • NICU
03

In context

Pain

2,450 studies on the registry are indexed under Pain; 945 are open to participants now.

This study's enrollment of 196 is above the median of 100 across 301 observational studies indexed under Pain.

Browse Pain studies →

Lead sponsor

Sanko University is the lead sponsor of 52 studies on the registry; 11 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
1 Day to 8 Days
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

The study included 196 newborns who were hospitalized in SANKO University Hospital Level 3 NICU and exposed to different painful procedures during routine clinical practices under Neonatologist follow-up.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Preterm and term infants admitted to the NICU for the first time for various reasons with a hospital stay ranging from 1 to 8 days
  • Preterm and term infants who were cared for in an incubator without any pharmacological or non-pharmacological analgesic therapy, muscle relaxant, and sedation treatment in the last 24 hours before the procedure.

Exclusion criteria

Exclusion Criteria:

  • Exposed to painful procedures more than 3 times in the same day
  • Infants who diagnosed with osteomyelitis, sepsis, pyejonic arthritis, congenital anomaly (Spina bifida, arthrogryposis multiplex congenita)
  • Infants with any known neurological diagnosis (Abnormal MRI finding, hydrocephalus, Chiari malformation, asphyxia, periventricular leukomolacia (PVL), acute bilirubin encephalopathy, hypoxic ischemic encephalopathy (HIE))
  • Infants who had any surgery
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
196 participants (actual)
Target follow-up
1 Week
Patient registry
Yes

Groups and cohorts

  • 1/Venous blood sampling

    The vessel was determined for cannulation and an anatomical tourniquet was applied. Skin antiseptic was prepared. The plastic wings of the winged angioket were held open. The skin over the vein to be accessed was stretched with the fingers of the free hand. The needle was inserted into the skin a few millimeters distal to the point to be inserted, and the blood was vascularized until the education. The cannula was advanced by retracting the stylet. The tourniquet was removed and the cannula was fixed.

  • 2/Heel puncture

    The skin was prepared with an antiseptic. The baby's heel was placed at an angle between the thumb and forefinger, with the other fingers grasping the ankle from behind. Pressure was applied to the back of the ankle with the other fingers by taking support against the thumb. The first drop of blood was wiped with sterile gauze by inserting the needle, and the next drops of blood were absorbed into the paper by touching the middle of the ring on the filter paper. An adhesive bandage was applied by applying pressure to the puncture site.

  • 3:Orogastric Catheter insertion

    The head of the bed was raised and the newborn was placed on his back. The midpoint distance from the tip of the nose to the ear, xiphoid and umbilicus was measured to determine the insertion length. With one hand, the infant's mouth was opened while his head was stabilized. With the other hand, the MV probe was advanced to the specified depth. The position of the OG probe was confirmed and fixed.

  • 4:Umbilical Catheter insertion

    The system was filled with liquid by connecting the tap to the UK. The faucet was turned off, sterile gauze was placed around the umbilical clamp and lifted out of the sterile area. The other assistant held the cord with a clamp and lifted it vertically up and away from the sterile field. The cord and its surroundings were prepared with an antiseptic solution and covered. The umbilicus was tied with a single knot and the cord was cut horizontally with a scalpel. Bleeding on the surface of the cord was wiped with sterile gauze. The cord stump was grasped with toothed forceps close to the vessel to be catheterized. The catheter was placed in the lumen of the vessel and advanced in the vessel. When the catheter exceeded 5 cm, it was aspirated to confirm the intraluminal position. The blood that came with an average of 0.5 ml bolus solution was cleaned and the catheter was fixed.

  • 5:Tracheal Intubation

    The head of the infant was positioned in the midline, slightly extended, with the chin up. The head was stabilized with the right hand by turning on the light of the laryngoscope. The blade of the laryngoscope was inserted by sliding the blade over the tongue until the tip of the blade rested on the Vallecula. The blade of the laryngoscope was slid up to open the mouth even more. The other assistant gently dipped it into the suprasternal notch. The concave edge of the tube was held with the right hand, and it was advanced approximately 2 cm, passing it between the vocal cords when the vocal cords and trachea were seen.

06

What researchers measure

Primary outcomes

  1. Neonatal Infant Pain Scale

    pain measurement of infants. This scale measures five behavioral groupings (i.e. facial expressions, crying, movements of arms and legs, and awake condition), and one physiological parameter (i.e. breathing patterns) given against pain during invasive procedures in preterm and term infants. The total score is between "0" and "7". The lowest pain level is 0, and the highest pain level is 7. The validity and reliability of the scale were shown in studies that were conducted with premature and term newborns.

    Time frame: The pain scale was scored in the first 5 minutes following the clinical procedure.

  2. O₂ saturation1

    O₂ saturation of the newborn 5 minutes before the painful procedure.

    Time frame: O₂ saturation value of the newborn 5 minutes before the painful procedure from the pulse oximeter.

  3. heart rate1

    the heart rate of the newborn 5 minutes before the painful procedure

    Time frame: the heart rate of the newborn 5 minutes before the painful procedure from the monitor

  4. heart rate2

    the heart rate of the newborn during the painful procedure

    Time frame: the heart rate of the newborn at the time point of the painful procedure from the monitor

  5. heart rate3

    the heart rate of the newborn 5 minutes after the painful procedure

    Time frame: the heart rate of the newborn 5 minutes after the painful procedure from the monitor

  6. O₂ saturation2

    O₂ saturation of the newborn during the painful procedure.

    Time frame: O₂ saturation of the newborn at the time point of the painful procedure from the pulse oximeter.

  7. O₂ saturation3

    O₂ saturation of the newborn 5 minutes after the painful procedure.

    Time frame: O₂ saturation of the newborn 5 minutes after the painful procedure from the pulse oximeter.

Secondary outcomes

  1. The type and Number of painful procedures

    The type and number of painful procedures will be recorded as Heel Puncture (HP), Venous Blood sampling (VB), naso and orogastric (NG-OG) catheter insertion, arterial blood collection, Tracheal Intubation (TI), several rectal procedures, the removal of adhesive tapes, insertion and removal of Umbilical Catheter (UC), and several other procedures such as aspiration, chest physiotherapy procedures,

    Time frame: The type and number of painful procedures during the first 8 days of life performed on newborns were also recorded.

  2. age (day)

    age of the infants will be recorded as day.

    Time frame: up to 7 days

  3. length (centimeter/cm)

    birth length of the infants

    Time frame: It will be recorded on the pain assesment day.

  4. gender

    gender of the infants will be recorde as f/m

    Time frame: up to 7 days

  5. Diagnosis of the infants (the reason for hospitalization of the infants)

    the reason for hospitalization of the infants will be recorded as Prematurity, Respiratuar Distress Syndrome (RDS), Bronchopulmonary Dysplasia (BPD), Low birth weight (LBW), Extreme low birth weight (ELBW), Sepsis, Patent Ductus Arteriosus (PDA), Retinopathy of Prematurity (ROP), Small for gestational age (SGA), Premature Rupture of Membranes (PROM).

    Time frame: up to 7 days

  6. the duration (day) of hospitalization of infants

    the duration of hospitalization of all infants will be recorded as day.

    Time frame: up to 7 days

  7. birth weight

    birth weight will be recorded in kilograms(kg)

    Time frame: at birth

07

Study locations

1 site
  • Hatice Adıgüzel
    Gaziantep, 27090, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 7, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05077345
Lead sponsor
Sanko University
Responsible party
Hatice Adiguzel, PT (Assistant Proffessor, Kahramanmaras Sutcu Imam University) — Principal investigator
First posted
Oct 14, 2021
Start date
Jan 15, 2019
Primary completion
Mar 25, 2020
Completion
Mar 30, 2020
Last update
Apr 7, 2022

Study contacts

hatice Adiguzel, PhD
principal investigator · Kahramanmaras Sutcu Imam University
mehmet Egilmez, PT
study chair · Sanko University
Nevin Ergun, Proffessor
study chair · Sanko University
Yusuf Unal Sarıkabadayi, Doctor
study chair · Sanko University
Bulent Elbasan, Proffessor
study director · Gazi University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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