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Pain clinical trials

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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.

NCT ID: NCT03450681 Completed - Pain Clinical Trials

Effectiveness of Pulsed Radiofrequency of the Saphenous Nerve in the Management of Knee Arthroplasty Pain

Start date: November 2014
Phase: N/A
Study type: Interventional

Approximately 40% of patients undergoing total knee arthroplasty develop acute to moderate post operative pain. Furthermore 20-30% develop chronic post operative pain. The objective of this work is to study the effectiveness and safety of pulsed radiofrequency of the saphenous nerve realized during the pre-operative period of total knee arthroplasty. The study design is a randomized, blinded clinical trial. Patients scheduled for total knee arthroplasty are divided into two groups. The first group procedure consists in pre-operative pulsed radiofrequency under ultrasound guidance of the saphenous nerve and standard postoperative pain management by the pain clinic. The second group receives only the standard postoperative pain management by the pain clinic. Patient follow ups are performed 3 times (after 2 weeks, 2 months and 6 months) within a period of 6 months, evaluating pain severity using the VAS.

NCT ID: NCT03445390 Completed - Pain Clinical Trials

The Effect of Intravenous Acetaminophen on Post-Operative Pain After Craniotomy

Start date: May 1, 2014
Phase: Phase 4
Study type: Interventional

The purpose of the study is to determine the efficacy of IV acetaminophen when administered to neurosurgical patients at the beginning and end of their surgery. If the result is improved pain control with less opioid consumption postoperatively, then those patients may also experience less opioid related side effects such as nausea/vomiting, pruritus, and sedation.

NCT ID: NCT03444493 Completed - Pain Clinical Trials

The Effect of Stabilization Exercises After Radiofrequency Lumbar Facet Denervation

Start date: February 15, 2015
Phase: N/A
Study type: Interventional

A gap of knowledge exists on the understanding of the acute effects of stabilization exercises on pain, disability and physical performance when applied after radiofrequency denervation. Therefore, the main objective of this study is to show the effects of stabilization exercises when started in acute period and also reduce the frequency of recurrence low back pain of patients with FJS after radiofrequency denervation.

NCT ID: NCT03438864 Completed - Pain Clinical Trials

Acute Effects of Interferential Current on Edema, Pain and Muscle Strength in Patients With Distal Radius Fracture

Start date: January 7, 2017
Phase: N/A
Study type: Interventional

Interferential current is a form of electrotherapy that is obtained by placing two different plates that produce medium frequency waveform current, resulting in a low frequency interferential waveform in deeper tissues. It was shown interferential current electrotherapy is beneficial for reduction of traumatic edema in tissues and pain control. Patients with conservatively managed distal radius fractures were recruited after casts are shed, and were treated with one session(30 minutes) of different protocols of interferential current electrotherapy. Before and after therapy, they were evaluated with volumetry, hand grip strength and visual analogue scale for pain.

NCT ID: NCT03428698 Completed - Pain Clinical Trials

Hyaluronic Acid and Amino Acid Gel Applied to the Alveolar Socket After Mandibular Third Molar Extraction

Start date: September 10, 2009
Phase: N/A
Study type: Interventional

Objective: The study aimed to assess the effect of topical application of an amino acid + sodium hyaluronate acid gel after lower third molar extraction. Study design: 136 patients requiring lower third molar extraction were enrolled. An amino acid + sodium hyaluronate acid (HA) gel was applied to the sockets of the patients in the treatment group immediately following extraction; the sockets of the controls were simply flushed with a sterile saline solution. 7 and 14 days after surgery, patients' outcomes and postoperative complications were evaluated. Cumulative incidence of dehiscence and secondary outcome measures were analyzed using a chi-square test.