Clinical Trial Details
— Status: Withdrawn
Administrative data
| NCT number |
NCT03718507 |
| Other study ID # |
SL2018PS |
| Secondary ID |
|
| Status |
Withdrawn |
| Phase |
Phase 1
|
| First received |
|
| Last updated |
|
| Start date |
May 20, 2019 |
| Est. completion date |
February 20, 2020 |
Study information
| Verified date |
July 2021 |
| Source |
ASST Fatebenefratelli Sacco |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Interventional
|
Clinical Trial Summary
Given the popularity that LISA technique has gainig in worldwide neonatal units, the lack of
evidence regarding its premedication is becoming even more relevant to provide the best care
to premature infants.
Objective of this clinical trial is to establish the best premedication for LISA procedure
considering neonatal pain assessed with premature infants pain scale, salivary cortisol
levels as an indicator of stress and crSO2 values as indicators of cerebral oxygenation.
Moreover, we aim to verify if sucrose 24% given orally is an effective tool for pain
management in preterm neonates also in more invasive procedure, comparable to pharmacological
treatment.
Description:
In the last decades, one of the most relevant interventions which have led to a significant
increase in preterm infants survival rate is the introduction of surfactant replacement
therapy.
Nowadays, given the trend towards the less invasive respiratory support also for low and
extremely low gestational age infants, the use of intubation and prolonged mechanical
ventilation has been minimized. In fact, bronchopulmonary dysplasia (BPD) has been proved to
be closely related to prolonged intubation and it is one of the main problem clinicians must
face with. This is the reason why the INSURE technique was introduced as a routine care
procedure in neonatal units. In fact, INSURE is the acronym for INtubation - SURfactant
administration-Extubation. This technique ensures the baby the positive effects of surfactant
on respiratory mechanics minimizing the intubation length. However, the INSURE procedure
still involves intubation, meaning that it is still invansive and some infants cannot be
extubated immediately afterward. Thus, lately new technique for surfactant administration has
been introduced. The most extensively studied are the so-called less invasive surfactant
administration (LISA) and minimally invasive surfactant therapy (MIST). With these
procedures, infants receive non-invasive continuous positive airway pressure (CPAP)
treatment, while being given intratracheal surfactant via a feeding tube or small catheter.
Although the paucity of literature available to date, for extremely preterm infants LISA has
shown to be able to reduce the need for intubation, ventilation and supplemental oxygen when
compared with the standard technique of rescue intubation and ventilation. In comparison with
the INSURE procedure the less invasive surfactant administration was associated with a
reduced need for ventilation and reduced risk of BPD.
Even if this technique can provide the gentlest treatment presently available in
administering surfactant, it implies laryngoscopy and somewhat discomfort. The importance of
proper care in managing preterm infants, especially during painful procedures, has been well
demonstrated and all the caregivers have to be even more committed to this aspect.
Pain in neonates is usually assessed through pain scales and using clinical parameters such
as pulse oximetry (SatO2) and Heart Rate (HR). Since pain scores are subject to caregivers'
individual perception and parameters can be influenced by other clinical underlying
condition, especially in preterm infants, determination of cortisol concentration could be a
useful alternative.
Cortisol is the major glucocorticoid produced in the adrenal cortex. Cortisol production has
a circadian rhythm, with levels peaking in the early morning and dropping to lowest values at
night. Levels rise independently of circadian rhythm in response to stress.
There is convincing evidence that providing neonates with oral glucose during painful
procedure reduces the stress related to the procedure itself, without serious side effects or
harms related to this intervention. Different concentrations of glucose solution are
currently available and have been used in neonatal field.
To date, there is still high debate on the need to provide sedation to babies undergoing
LISA, and lack of evidence available regarding the optimal premedication. Some Authors report
to use LISA technique without any sort of sedation, while others perform it with the same
sedation they use for INSURE method.
Moreover, there is lack of evidence in regard to the effects of this method on cerebral
oxygenation, which can be easily monitored using NIRS (near infrared spectroscopy).
Since LISA technique's popularity is increasing, we believe that there is urgent need to
better clarify how this approach can be performed in the gentlest way.
Given these premises, we indeed speculate that oral glucose as a premedication for LISA
procedure could be an intriguing alternative to standard sedation.
Objective of this clinical trial is to establish the best premedication for LISA procedure
considering neonatal pain assessed with premature infants pain scale, salivary cortisol
levels as an indicator of stress and crSO2 values as indicators of cerebral oxygenation.
Moreover, we aim to verify if sucrose 24% given orally is an effective tool for pain
management in preterm neonates also in more invasive procedure, comparable to pharmacological
treatment.
Evaluation of the efficacy of non-pharmacological sedation will lead to:
- a gentler approach for preterm babies and a better understanding of LISA technique
- an improvement in pain management, where sucrose can be applied for several painful
procedures of different degrees of invasiveness, not only in the mildest ones
- a significant reduction in prolonged ventilation due to surfactant administration's
pharmacological sedation
- a safer use of surfactant administration also in level II neonatal unit, since the risk
for subsequent need of invasive respiratory support due to excessive sedation would be
considerably reduced
- a significant economic impact on public health care system, for the inferior cost of
oral sucrose
- a relevant decrease of the onset and subsequent public cost of BPD, if data about LISA
technique capability to reduce it will be further confirmed.
- Primary Outcome:
Verify which is the best premedication for LISA procedure to reduce neonatal pain.
- Secondary Outcomes:
- Verify the effects of different forms of premedication on cerebral oxygenation during
LISA procedure
- Verify the effects of different forms of premedication on cortisol levels before and
after LISA procedure
- Verify the efficacy of sucrose 24% in pain control during more invasive procedures
- Verify the influence of premedication on adverse events' occurrence during LISA
procedure
- Verify the effects of different pre-medications on the ease in administering surfactant
with LISA technique (time required, number of attempts, …)
Trial Design:
An investigator-initiated randomized, single center, pilot study that will enroll 20 preterm
neonates between 27 and 29+6 weeks of gestation.
Multiple births will be randomised into the same treatment arm.
Trial Interventions:
- Study group 1: patients will receive atropine (0.01-0.02 mg/kg i.v. bolus) and fentanyl
(0.5-2 mcg/kg i.v. in 5 minutes) before LISA in addition to standard care (wrapping).
NIRS will be monitored during the whole procedure
- Study group 2: patients will be given atropine (0.01-0.02 mg/kg i.v. bolus) and oral
sucrose 24% (0.5 ml) 2 minutes before LISA in addition to standard care (wrapping). NIRS
will be monitored during the whole procedure.
All the procedure will be videorecorded and subsequently analyzed
