Benefit & Tolerability of a Probiotic Product in Infants With Abdominal

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Abdominal Discomfort

See also
	Status	Clinical Trial	Phase
	Completed	`NCT01064661` - Pilot Study Studying Physiological Effects of Probiotic Pills in Patients With Abdominal Pain/Discomfort and Bloating	N/A
	Completed	`NCT01099696` - Study to Evaluate a Probiotic in Healthy Subjects With a History of Abdominal Discomfort and Bloating	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT01064661 - Pilot Study Studying Physiological Effects of Probiotic Pills in Patients With Abdominal Pain/Discomfort and Bloating

N/A

Completed

NCT01099696 - Study to Evaluate a Probiotic in Healthy Subjects With a History of Abdominal Discomfort and Bloating

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT01893814
Study type	Interventional
Source	Probi AB
Contact
Status	Terminated
Phase	Phase 2
Start date	April 2013

Benefit and Tolerability of a Probiotic Product in Infants With Abdominal Discomfort

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms