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Colic clinical trials

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NCT ID: NCT00929292 Completed - Growth Clinical Trials

Safety and Tolerance Study of Alpha-Lactalbumin Enriched and Probiotic-Supplemented Infant Formula in Infants With Colic

Start date: November 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the nutritional adequacy, the digestive tolerance and the effect on colic of an alpha-lactalbumin-enriched and probiotic-supplemented infant formula.

NCT ID: NCT00922727 Completed - Colic Clinical Trials

Safety of Lactobacillus Reuteri (L. Reuteri) in Healthy Adults

Start date: October 2009
Phase: Phase 1
Study type: Interventional

This study will evaluate the safety and tolerability of the probiotic Lactobacillus reuteri (LR) in healthy adult patients. Patients will be randomized to receive either LR or placebo orally each day for a total of 60 doses. The effects on fecal bacteria, circulating white blood cell receptors and inflammatory cytokine profiles will be measured.

NCT ID: NCT00907621 Completed - Infant Colic Clinical Trials

Effects of Acupuncture in the Treatment of Infant Colic

Start date: September 2009
Phase: Phase 2
Study type: Interventional

Standardized acupuncture treatment for infant colic is a common treatment in general practice for doctors educated in medical acupuncture. The investigators plan to study whether the perceived opinion on positive results can be verified in a multi-center clinical trial. The investigators aim to measure the effect of standardized acupuncture treatment, three repeated sessions, on infant colic in a randomized singe blinded prospective multi-center study, starting September 2009. The study will be done in thirteen locations in Norway by specialists in General Practice trained in acupuncture. The investigators intend to include a total of 130 patients, 65 in the intervention group and 65 in the control group.

NCT ID: NCT00860301 Completed - Infantile Colic Clinical Trials

Acupuncture in Infantile Colic

Start date: December 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate whether acupuncture influences: - the rate of infants who still fulfil the colic criterion after three intervention weeks - the time when the infants are crying, fussing or have intense bouts of colicky symptoms

NCT ID: NCT00796523 Completed - Colic Clinical Trials

An Intervention to Decrease Infant Crying

Start date: August 2005
Phase: N/A
Study type: Interventional

This is a study looking at the Happiest Baby on the Block technique. The investigators hypothesized that infants of mothers given a 30 minute videotape demonstrating the Happiest Baby on the Block technique would fuss/cry less and sleep longer than infants of mothers given a 30 minute videotape on general newborn care. The investigators also hypothesized that mothers given the Happiest Baby on the Block videotape would have lower levels of stress.

NCT ID: NCT00655083 Completed - Infantile Colic Clinical Trials

A Phase I Study to Evaluate the Oral Absorption of Nepadutant in Infants

Start date: March 2008
Phase: Phase 1
Study type: Interventional

The purpose of the study is to evaluate the gastrointestinal absorption of nepadutant after single dose as oral solution (and the effect of age on its oral absorption) in infants. Oral absorption is evaluated through the drug recovery in urine.

NCT ID: NCT00646061 Completed - Renal Colic Clinical Trials

Pain Control in Renal Colic

Start date: November 2007
Phase: Phase 1
Study type: Interventional

Renal colic is very common in emergency department patients. Our aim of this study is which combination of drug is more effective in renal colic.

NCT ID: NCT00177086 Completed - Kidney Calculi Clinical Trials

Alfuzosin Hydrochloride to Promote Passage of Distal Ureteral Calculi

Start date: September 2005
Phase: Phase 3
Study type: Interventional

This study will assess improvement in the percentage of spontaneous stone passage for distal ureteral calculi for alfuzosin compared to placebo, decrease of pain and narcotic/analgesic use associated with stone passage, decrease of the time to spontaneous stone passage, shift in the size distribution of stones passed towards larger sizes.