Probiotic
Dietary SupplementSingle strain probiotic in a form of a sachets with a daily dose of 1.0E+9 Colony Forming Unit (CFU) per day for 4 weeks
NCT Number: NCT05432479
This study evaluates the efficacy of single strain probiotic administered in a form of a sachet in the treatment of infant colic in infants 3-12 weeks old.
Interested in participating?
Request Info3 week–12 week
All sexes
Interventional
Not applicable
Pulse Multispeciality Hospital,, Pune, Maharashtra, India
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Single strain probiotic in a form of a sachets with a daily dose of 1.0E+9 Colony Forming Unit (CFU) per day for 4 weeks
Placebo
Time frame: Day 0 , Day 28
eDiary parent reported cry and fuss time
Time frame: Day 0, Day 28
Reduction of cry and fuss time (parent reported) greater than 90% comparing to baseline
Time frame: Day 0, Day 28
eDiary parent reported cry and fuss bouts
Time frame: Day 0 Day 28
eDiary parent reported sleep time
Time frame: Day 0, Day 28
Change in the proportion of participants needing to use rescue medications between the study arms
Time frame: Day 0, Day 28
Change in maternal QoL using WHO QOL/BREF (improvement marked by increase in the total score)
Time frame: Day 0, Day 28
Change in maternal QoL using MMPP/QoL (improvement marked by increase in the total score)
Contact information is provided by the study sponsor or research team.
The Archer-Daniels-Midland Company
Industry
A Randomized, Double-blinded, Placebo-controlled Study to Evaluate the Efficacy of a Probiotic in Infantile Colic Symptoms Relief
Acronym: PIXAR
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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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