Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04440462
Other study ID # RC 13/2019
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 18, 2020
Est. completion date December 31, 2024

Study information

Verified date June 2024
Source IRCCS Burlo Garofolo
Contact Milena Cadenaro, DDS MSc PhD
Phone +390403785675
Email milena.cadenaro@burlo.trieste.it
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Ankyloglossia (tongue-tie) is a congenital anomaly characterized by a short lingual frenulum that limits the physiological tongue movement and occurs with an estimated prevalence between 4 and 10% of the newborns. This condition can be associated with difficulty in breastfeeding which can be painful for the mother, dysfunctional swallowing and future speech difficulties. The prevalence of nipple pain among women breastfeeding newborns with ankyloglossia is estimated to be between 36 and 80%. Since an early intervention can prevent the difficulties that may occur during the child's growth and can also improve the mothers and patients' quality of life, it is important to evaluate the lingual frenulum in the first days of life. The treatment of ankyloglossia consists in the frenulotomy which allows the release of the lingual frenulum and is a relatively simple procedure with few side effects and minimal post-operative. Different methods performed with or without local anaesthesia by means of scissors, blade, laser (etc.) are described in literature for the procedure the newborn. The hypothesis of the study is that the addition of a water and sugar solution to the standard analgesia with lidocaine may lead to a greater benefit in terms of pain control and determine the activation of different brain areas. The primary aim of the study is to evaluate whether the administration of a water and sugar solution to newborns undergoing frenulotomy receiving topical lidocaine as standard analgesic protocol, may lead to an additional benefit in terms of pain reduction evaluated according to the Neonatal Infant Pain Scale (NIPS). The secondary aim of the study is to evaluate through a Hitachi multichannel near-infrared spectroscopy (NIRS) the effects of the addition of a water and sugar solution to the standard analgesic protocol with topical lidocaine on the cortical activation.


Recruitment information / eligibility

Status Recruiting
Enrollment 72
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 1 Day to 10 Days
Eligibility Inclusion Criteria 1. Term newborns (37 - 41 weeks of gestational age) within the first 10 days of life; 2. Birth weight = 2500 grams; 3. Presence of ankyloglossia; 4. Indication to the frenulotomy according to the Hazelbaker Assessment Tool for Lingual Frenulum Function (HATLFF): anatomical-functional evaluation with a score lower than 8. Exclusion Criteria: 1. Syndromic diagnosis (genetic/hereditary); 2. Pathology of main organ (heart disease, brain disease etc.); 3. Drugs intake that may interfere with the collected data (sedatives).

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Sugar and water solution
2 ml of a water and sugar solution (3 full-teaspoons of granulated sugar dissolved in half glass of water)
Sterile water
2 ml of sterile water

Locations

Country Name City State
Italy Institute for Maternal and Child Health - IRCCS Burlo Garofolo- Trieste

Sponsors (1)

Lead Sponsor Collaborator
IRCCS Burlo Garofolo

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain reduction The perception of pain in newborns will be evaluated according to the Internationally Validated Neonatal Infant Pain Scale (NIPS).This scale detects the presence of six behavioral expression signs of neonatal pain (facial expression, crying, respiratory pattern, arms and legs' activity, arousal state) and ranges from 0 (absence of pain) to 7 (maximal pain level). 30 seconds after the frenulotomy
Secondary Pain reduction The perception of pain in newborns will be evaluated according to the Internationally Validated Neonatal Infant Pain Scale (NIPS).This scale detects the presence of six behavioral expression signs of neonatal pain (facial expression, crying, respiratory pattern, arms and legs' activity, arousal state) and ranges from 0 (absence of pain) to 7 (maximal pain level). During the frenulotomy
Secondary Cortical oxy-haemoglobin change Multichannel near-infrared spectroscopy will be used to estimate cerebral cortex activation by measuring increase in cortical oxy-haemoglobin (HbO2) (Hitachi multichannel NIRS system) 30 seconds after the frenulotomy
See also
  Status Clinical Trial Phase
Recruiting NCT05560750 - Lingual Frenulum in Newborn Infants (LINNE) N/A