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Pain clinical trials

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NCT ID: NCT03584880 Completed - Pain Clinical Trials

Postoperative Pain After Root Canal Disinfection Via Diode Laser

Start date: February 8, 2018
Phase: N/A
Study type: Interventional

The prevention and control of post-treatment pain is of great importance for the comfort of the patient as well as for the clinician's prestige. In this study, the effect of 940 nm diode laser disinfection on the postoperative pain of retreatment cases was evaluated.

NCT ID: NCT03571009 Completed - Pain Clinical Trials

Real-time Pain Monitoring in Fibromyalgia Patients

Start date: December 22, 2015
Phase: N/A
Study type: Interventional

This study aims to examine whether the pain of fibromyalgia patients can be reduced with utilization of real-time pain monitoring system (PAAS). In this pilot study, adult fibromyalgia patients were randomly assigned to use or to not use PAAS. Changes in the visual analogue scale (VAS) were examined by rheumatologists at baseline and after three months, and correlations between conventional pain VAS or PAAS VAS and clinical parameters (patient global assessment, physician global assessment, fibromyalgia impact questionnaire) were investigated. We also examined if the utilization of PAAS can affect health related quality of life and depression.

NCT ID: NCT03568721 Completed - Pain Clinical Trials

Postoperative Effects of Chewing Gum, Ibuprofen and Acetaminophen on Pain After Initial Archwire Placement

Start date: January 25, 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the efficacy of ibuprofen, acetaminophen, chewing gum and placebo in reducing orthodontic pain. this study include 92 patients to be classified into 4 groups of 23 each: ibuprofen (400 mg), acetaminophen (500 mg), chewing gum and control. The patients in each group will receive 1 method immediately after placement of the initial archwire and every 6 hours for a week if they experiences pain. Pain perception will be recorded by the patients while jaw rest position and fitting back teeth at 24 hours, 2 days, 3 days, 7 days and 21 days after archwire placement, using a visual analog scale.

NCT ID: NCT03541538 Completed - Pain Clinical Trials

Hypoalgesic Effect of Cervical Manipulation

Start date: May 20, 2017
Phase: N/A
Study type: Interventional

This study evaluates the hypoalgesic effect of global and specific cervical joint manipulation in healthy individuals. At first the participants received one of the interventions and after 48 hours, the other.

NCT ID: NCT03534999 Completed - Hip Fractures Clinical Trials

Transcutaneous Electrical Nerve Stimulation on Pain Intensity of Patients With Hip Arthroplasty

Start date: October 2, 2017
Phase: N/A
Study type: Interventional

Fifty patients with hip arthroplasty were purposively recruited for the study. They were allocated into two groups randomly with equal number. One group had TEN, other served as control. Pain intensity was measured every day of the treatment.

NCT ID: NCT03486015 Completed - Pain Clinical Trials

Oral Sweet Solution to Prevent Pain During Neonatal Hip Examination

Start date: March 1, 2016
Phase: N/A
Study type: Interventional

This study evaluates the pain relieving effect of oral glucose during hip examinations on healthy, fullterm infants.

NCT ID: NCT03478241 Completed - Pain, Postoperative Clinical Trials

Postoperative Pain Intensity Associated With the Use of Different Nickel Titanium Instrumentation Systems

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

In this study the effect of different engine-driven nickel titanium (Ni-Ti) instrumentation systems (OneShape, Revo S and WaveOne) on postoperative dental pain in patients with asymptomatic teeth after a single-appointment root canal retreatment was evaluated.

NCT ID: NCT03470532 Completed - Pain Clinical Trials

Comparing Articaine and Mepivacaine Without Palatal Injection in Pain Assessment During Maxillary Teeth Extraction

Start date: February 25, 2017
Phase: Phase 4
Study type: Interventional

This study compares the the efficacy of buccal infiltration of 4% Articaine and 2% Mepivacaine without any palatal injection during extraction of maxillary teeth. One group of patient receives buccal infiltration of Articaine and another group receives buccal infiltration of Mepivacaine.

NCT ID: NCT03468270 Completed - Pain Clinical Trials

Pain Coping Strategies in Children With CP

Start date: July 1, 2013
Study type: Observational

The aim of the study is to describe pain coping strategies and their evolution in children and adolescent with cerebral palsy.

NCT ID: NCT03459872 Completed - Pain Clinical Trials

Acupuncture Outcomes Based Rehabilitation

Start date: September 28, 2016
Phase: N/A
Study type: Observational [Patient Registry]

Can acupuncture be quantified. This study sets out to observe if there are measurable effects of fine motor control that are attributable to acupuncture. The study utilizes an FDA approved medical device for measurements of fine motor control called the RU-Fit.