Colic, Infantile

3

Review clinical trials related to Colic, Infantile. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Effect of Probiotic Limosilactobacillus Reuteri (L. Reuteri) on Crying Time in Infants With Colic

This is a double-blind, multi-center, randomized, placebo-controlled, parallel-group study in infants with colic with the primary objective to evaluate crying time.

Participants needed: 102
Trial details
Age: 3-8Biological sex: AllType: InterventionalSponsor: BioGaia ABUpdated: Sep 22, 2025Locations: 2
Eligibility criteria

Aged between 3-8 weeks at screening. [+11]

Infants with severe gastroesophageal reflux (throwing up or spitting up more tha... [+5]

Status: Not yet recruiting

Validation Of A Parent Administered Symptom Score For Unsettled Infants (Every Baby is UnIQue)

It's common for infants to be unsettled, especially in the first few months of life. While this is often normal, persistent symptoms can be stressful for families. Parents naturally seek explanations, and common suspected causes include colic, reflux, eczema, and cow's milk allergy (CMA). However, CMA is frequently over diagnosed, which can lead to unnecessary changes such as stopping breastfeeding or switching to expensive specialist formulas. To address this, we've developed an online questionnaire to help track and understand symptoms in unsettled infants. Our long-term goal is to use this tool to support more accurate diagnosis of CMA. Before that, we need to test and validate the questionnaire in a general population of infants, including those who are healthy and those with other temporary conditions like a recent immunisation or teething. This study involves an anonymous online survey for parents of babies under 12 months old. We aim to collect data from approximately 350 participants. The study will help us assess how well the questionnaire reflects the severity of symptoms and whether it can distinguish between healthy infants and those with underlying issues. Parents will be invited to take part using flyers with a QR code distributed in various healthcare settings, including GP clinics and children's clinics in hospital. The survey is anonymous and hosted on a secure platform. While we don't anticipate the questions to be distressing, we recognise some may touch on sensitive topics. Support resources and study team contact details will be provided. By validating this tool, we hope to improve how unsettled behaviour in infants is assessed-reducing unnecessary interventions and better supporting families and healthcare professionals.

Participants needed: 350
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University Hospital Southampton NHS Foundation TrustUpdated: Aug 13, 2025Locations: 1
Eligibility criteria

Consent to complete the anonymous questionnaire [+2]

Parent does not consent to complete the anonymous questionnaire [+2]

Status: Recruiting

Prevalence and Natural History of Functional Gastrointestinal Disorders Among At-risk Infants.

The goal of this observational study is to learn about the prevalence and characteristics of functional gastrointestinal disorders (FGID) in at risk infants (former preterm infants and those with birth asphyxia) during the first 2 years of life. The main questions it aims to answer are: * evaluate the prevalence of symptoms related to gastro-esophageal reflux (GER), of functional gastrointestinal disorders during the first 2 years of life * describe growth parameters during follow-up up to the corrected age of 2 years Participants will be assessed clinically and with a structured questionnaire based on the Rome IV criteria to describe FGID.

Participants needed: 71
Trial details
Age: 3-24Biological sex: AllType: ObservationalSponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCSUpdated: Mar 11, 2025Locations: 1
Eligibility criteria

infants with gestational age at birth < 31 weeks [+2]

lack of informed consent [+1]