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Colic clinical trials

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NCT ID: NCT02878148 Completed - Nephrolithiasis Clinical Trials

Conditional Imaging Prescription Strategy for Exploration of Acute Uncomplicated Renal Colic

IMAGENCO
Start date: October 17, 2016
Phase: N/A
Study type: Interventional

Prospective single centre study aiming at validating a conditional imaging strategy for diagnosis of suspected kidney stone. Consecutive Emergency department patients referred to the medical imaging department for exploration of a suspected acute uncomplicated renal colic will undergo the following interventions : systematic plain abdominal Xray, systematic ultrasonography and systematic unenhanced CT (with a reduced dose scan), in addition to clinical examination and assessment of body mass index and the Sex, Timing, Origin, Nausea, Erythrocytes (STONE) clinical prediction score for symptomatic stone. Patients will be followed up at 1 month to record the need for urologic intervention and its type. The performances of different conditional imaging strategy for the diagnosis of suspected renal colic will be assessed retrospectively. The conditional strategies tested will be based on the patient's stone score and BMI and targeted use of combined plain X-ray and ultrasonography and/or unenhanced CT. The reference diagnosis for renal colic will be made according to the finding of a ureteral stone or indirect signs of urolithiasis at unenhanced CT.

NCT ID: NCT02865564 Completed - Clinical trials for Gastrointestinal Diseases

Effect of Lactobacillus Reuteri DSM17938 in Neonates Treated With Antibiotics

Start date: November 2016
Phase: N/A
Study type: Interventional

The aim of the study is to elucidate the relationship between postnatal antibiotic administration on development of gut microbiota and possible protective influence of simultaneously administration of probiotic during antibiotic therapy on development of gut microbiota, functional gastrointestinal disorders of infancy, weight gain and body composition.

NCT ID: NCT02839239 Completed - Infant Colic Clinical Trials

Lactocare Baby Drops in Infants Colic

LACONIC
Start date: December 9, 2016
Phase: N/A
Study type: Interventional

The objective of this study is to determine an efficacy of the combination of L. rhamnosus 19070-2 (FloraActiveTM) and L. reuteri DSM 122460 (FloraActiveTM) in decreasing cry/fuss in infants aged 4 through 12 weeks with IC. The active group of infants will receive lactobacilli with vitamin D3 while the control group will receive vitamin D3 2 times daily as oil suspension for 28 days. Duration of infant fuss/cry will be measured at baseline and at the end of intervention to define a difference between the groups

NCT ID: NCT02781415 Completed - Renal Colic Clinical Trials

Acupuncture Versus Titrated Morphine in Patients With Renal Colic

AcuRC
Start date: July 2014
Phase: Phase 3
Study type: Interventional

The aim of this study is to compare the clinical efficacy and safety profiles of a 30 minutes acupuncture session performed at an ER of a tertiary hospital versus titrated intravenous morphine in the management of acute severe pain syndromes (defined as a visual analogue scale (VAS) score >/= 70) taking for example acute renal colic.

NCT ID: NCT02727530 Completed - Infant Colic Clinical Trials

The Effectiveness of the Manual Therapy on Infant Colic (MT-IF)

Start date: April 2016
Phase: N/A
Study type: Interventional

The main goal of this study is to get to know if applying manual therapy will reduce the infant colic symptoms for to improve quality of life of babies and parents.

NCT ID: NCT02708238 Completed - Infantile Colics Clinical Trials

Efficacy of Matricariae Chamomilla L., Melissa Officinalis L. and Tyndallized Lactobacillus Acidophilus (H122) for Infantile Colics

Start date: April 2014
Phase: Phase 4
Study type: Interventional

A multicenter prospective, randomized comparative study will be conducted in infants with colic, according to Rome III criteria. Enrolled infants will be assigned at random to receive Chamomilla L., Melissa Officinalis L. and tyndallized L. Acidophilus (H122), L reuteri DSM 17938 (108 CFU) or simethicone. Treatment will be given to subjects for 28 days and they will be followed for 4 weeks. Treatment success will be assessed at the end of study period. Daily crying and fussing times will be recorded in a structured diary, and maternal questionnaires will be completed to monitor changes in infant colic symptoms and adverse events.

NCT ID: NCT02595515 Completed - Infantile Colic Clinical Trials

The Effect of Chiropractic Treatment of Infantile Colic

Start date: November 2015
Phase: N/A
Study type: Interventional

Infantile colic is condition that affects more than 10% of babies and their families. The reason, and hence proper treatment, for this condition is unknown and many causes have been suggested. One of the treatments that parents choose is chiropractic manipulation. In Denmark, almost 10,000 babies are each year treated by chiropractors, and a high proportion is due to colic. However, the effect of chiropractic treatment of infantile colic has not been properly scientifically evaluated. The effects of chiropractic treatment on infantile colic needs to be investigated, since this is a very common disorder with no known effective treatment, but with good empirical evidence of the value of chiropractic treatment. Although it is usually considered to be a benign and self-limiting condition, some studies suggest there might be long-term effects in terms of psychomotor problems. In worst case, the infants' crying may also lead to violence and 'shaken baby syndrome'. Null hypothesis: There is no effect of chiropractic treatment on the course of infantile colic. This study is a controlled, clinical trial where infants fulfilling the diagnostic criteria for colic will be randomized into two groups. One group will receive treatment and the other won't. This will determine the overall effect and furthermore, subgroup analyses will be performed to identify possible subgroups of infants, who will benefit the most from the treatment.

NCT ID: NCT02304783 Completed - Renal Colic Clinical Trials

Oral NSAI Versus Paracetamol or Placebo as a Second Line Treatment for Renal Colics

ONSAIP-RC
Start date: January 2014
Phase: Phase 3
Study type: Interventional

Outpatients treatment with NSAI in renal colics has not been well investigated and there is no clear recommendations regarding this matter. The aim of this study is to determine if an oral NSAI treatment is beneficial in patients discharged for the emergency departement after the first line treatment of a renal colic investigating the recurrence of pain, the reconsultation rates and the admissions.

NCT ID: NCT02268955 Completed - Biliary Colic Clinical Trials

Analgesic Efficacy of Intravenous Ibuprofen in Biliary Colic

Start date: September 9, 2014
Phase: N/A
Study type: Interventional

The aim of this study is to assess the analgesic efficacy of intravenous ibuprofen given in the Emergency Department for the treatment of biliary colic. We hypothesize that intravenous ibuprofen will provide a clinically significant drop in self-reported patient pain level as measured by the visual analog scale.

NCT ID: NCT02242292 Completed - Colic Clinical Trials

Study to Evaluate Efficacy and Safety of Oral Doses of Hyoscine Butylbromide for the Treatment of Occasional Abdominal Pain, Cramping, and Discomfort

Start date: April 2006
Phase: Phase 2
Study type: Interventional

Study to determine whether hyoscine butylbromide can provide adequate symptomatic relief of a single episode - defined as lasting not longer than 1 day - and multiple episodes of abdominal pain or discomfort associated with cramping when used as needed