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Colic clinical trials

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NCT ID: NCT03939611 Completed - Infantile Colic Clinical Trials

The Effect of Foot Reflexology on Infantile Colic Symptoms

Start date: June 26, 2016
Phase: N/A
Study type: Interventional

Aim: To compare the effect of foot reflexology and placebo foot reflexology on colic symptoms such as pain, ineffective sleep, and colicky crying periods in infants with colic. Method: The study was conducted as a single-blind, randomized, placebo-controlled trial in a child hospital between June 2016 and March 2017. To start with, 20 infants with colic were randomly selected for the reflexology group, and 25 babies with colic were randomly selected for the placebo group. Simple randomization was used; the parents and statistician were blinded to group assessment. The researcher could not be blinded because of the role played in the study. Foot reflexology was implemented with reflexology-group infants. Placebo foot reflexology was used with placebo-group infants. Both interventions were performed four times, for 20 minutes, each, by the researcher over the course of two weeks. The data were collected by the researcher using the information form, infantile colic scale, behavioral pain scale, crying and sleeping follow-up forms.

NCT ID: NCT03877458 Completed - Infantile Colic Clinical Trials

Combined Probiotics is More Effective in the Treatment of Infantile Colic

Start date: February 16, 2017
Phase: N/A
Study type: Interventional

All participants are randomized into 1 of 3 treatment arms, the mixture L acidophilus, B longum and B. bifidum group, Lactobacillus reuteri or placebo group. Primary outcome is defined as a reduction in the duration of average crying and fussing times, from baseline (day 0) to age 6 months, to <3 hours per day. Secondary outcome are the number of participants who respond to treatment on days 7, 14, 21, 28 and each month till age 6 months.

NCT ID: NCT03865004 Completed - Renal Colic Clinical Trials

Combination Trial of Intravenous Paracetamol - Morphine for Treating Acute Renal Colic in Emergency Setting: An Optimum Treatment

Start date: October 17, 2015
Phase: Phase 4
Study type: Interventional

This randomized, placebo-controlled trial evaluated the analgesic efficacy and safety of intravenous morphine-paracetamol combination and morphine-dexketoprofen combination morphine for the optimum treatment of renal colic. Combination of IV morphine and paracetamol is as effective and rapid as combination of IV Morphine and IV dexketoprophen for optimum treating of renal colic.

NCT ID: NCT03780556 Completed - Renal Colic Clinical Trials

Lornoxicam With Low Dose Ketamine Versus Pethidine to Control Pain of Acute Renal Colic

Start date: January 2, 2016
Phase: N/A
Study type: Interventional

Patients with acute renal colic divided into 2 groups. Group L administered ornoxicam and Group P administered pethidine and VAS was recorded for both groups.

NCT ID: NCT03706404 Completed - Renal Colic Clinical Trials

Renal Colic Fast Track Pathway in the Emergency Department.

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

Validation of a high-resolution, fast track pathway that combines the use of laboratory tests at the Point-of-Care Testing (POCT) and Point-of-Care ultrasound (POCUS) versus the classical pathway, in which blood samples are sent to the central laboratory and comprehensive radiological exams ordered, being equally effective, at a lower cost of care and time of stay in the emergency department.

NCT ID: NCT03704623 Completed - Ureteric Stone Clinical Trials

Parecoxib vs Paracetamol in the Treatment of Acute Renal Colic

Start date: May 1, 2019
Phase: Phase 4
Study type: Interventional

This study will be conducted to compare the efficacy and safety of Parecoxib versus Paracetamol for treatment of acute renal colic due to ureteric stones.

NCT ID: NCT03675763 Completed - Clinical trials for Gastro-Intestinal Disorder

Efficacy of a Craniosacral Therapy Protocol in the Treatment of Infant Colic

Start date: March 2, 2015
Phase: N/A
Study type: Interventional

This is a randomised controlled trial that aims to determine the effectiveness of craniosacral therapy for the treatment of infantile colic. Manual therapy was applied to a group of young infants diagnosed with colic while a second group did not received any treatment.

NCT ID: NCT03665753 Completed - Pain Clinical Trials

Comparison of IV 10, 20, and 30mg for Renal Colic Pain in the ED

Start date: November 5, 2018
Phase: Early Phase 1
Study type: Interventional

Hypothesis: Intravenous administration of Ketorolac 10 mg and 20 mg is as effective as 30 mg in treating renal colic pain in patients presenting to the emergency department

NCT ID: NCT03638921 Completed - Renal Colic Clinical Trials

35RC17_8826_NEPHROPAIN Phase APRES : Interest of the Equimolar Oxygen Nitride Mixture (MEOPA) in the Treatment of Pain in Patients Presenting to the Emergency Department for Suspected Renal Colic: a Study BEFORE AFTER

NEPHROPAIN
Start date: October 1, 2018
Phase: Phase 2
Study type: Interventional

MEOPA (Equimolar Oxygen-Nitrogen Protoxide Mix) is a gas used in emergencies for short-term painful acts. It is often very effective with an analgesic, anxiolytic and muscle relaxant action. It is often combined with other analgesic medicines. It has already been proven in emergency medicine for short-term pain and trauma. It seems that it could be used more particularly for pains of medical origin. A study has already proved its effectiveness in the treatment of migraines in emergencies. The first phase of the NEPHROPAIN study began in 2016 after a favorable opinion from the Regional Ethics Committee. NEPHROPAIN phase AVANT was a prospective non-interventional study on the use of analgesic drugs in nephritic colic in emergencies by Dr. Alexandre Tanneau. This study was conducted at the University Hospital of Rennes and included 60 patients admitted to the emergency department for suspected renal colic. It made it possible to recruit the control group of the NEPHROPAIN study. Its main objective was to describe the suspected population of renal colic in Rennes emergencies, to determine NEPHROPAIN's primary endpoint and the number of NEPHROPAIN needed subjects.

NCT ID: NCT03617289 Completed - Renal Colic Clinical Trials

Efficacy of Magnesium Sulfate on Reducing Renal Colic in the Emergency Department

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

To determine if magnesium sulfate paired with an analgesic medication will improve patient pain from renal colic compared with analgesic alone.