University of Salento, University Hospital Vito Fazzi Lecce
Lecce, LE, 73100, Italy
NCT Number: NCT06462651
This is a double-blind, randomized, placebo-controlled, parallel-group study in infants with colic with the primary objective to evaluate crying and fussing time.
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Notify Me3 week–12 week
All sexes
Interventional
Not applicable
Lecce, LE, 73100, Italy
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Supplementation with drops containing L. reuteri once daily for 21 consecutive days
Supplementation with identical drops without L. reuteri once daily for 21 consecutive days
Time frame: [Time Frame: From baseline to Day 7]
To evaluate crying and fussing time after 7 days of supplementation with L. reuteri in infants with colic.
Time frame: [Time Frame: From baseline up to Day 21]
Change in mean daily crying and fussing time measured by Baby´s Day Diary
Time frame: [Time Frame: From baseline up to Day 21]
Change in mean daily crying time measured by Baby´s Day Diary
Time frame: [Time Frame: From baseline up to Day 21]
Proportion of responders defined as reduction of daily average crying time with 50 % compared to baseline
Time frame: [Time Frame: From baseline up to Day 21]
Change in family QoL measured by the PedsQL Family Impact Module (Acute) - Total Score
Time frame: [Time Frame: From baseline up to Day 21]
Change in mean sleeping time measured by Baby´s Day Diary
Time frame: [Time Frame: From baseline up to Day 21]
Change in maternal depression measured by the Edinburgh Postnatal Depression Scale Total Score
BioGaia AB
Industry
A Double-blind, Randomised, Placebo-controlled, Parallel-group Study Evaluating the Effect of Probiotic Limosilactobacillus Reuteri (L. Reuteri) on Crying and Fussing Time in Infants With Colic
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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