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Pain clinical trials

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NCT ID: NCT02595190 Recruiting - Pain Clinical Trials

Treatment of the Symptomatic Sacral Perineurial Cysts

TSSPC
Start date: March 2015
Phase: Phase 4
Study type: Interventional

There are very few data and analysis in the literature regarding the symptomatic sacral perineurial cysts. Most studies are case reports or small retrospective sample, which rarely more than 20 cases. There is no an consensus on the choice of treatment (medicine conservative treatment and surgical treatment) for symptomatic sacral perineurial cysts.Our aim, therefore, is to compare the efficacy of medicine conservative treatment and surgical treatment for symptomatic sacral perineurial cysts by a randomized controlled trial. Meanwhile, resting-state functional magnetic resonance imaging is used to detect the changes at pain related brain areas, which will be develop an objective method to evaluate the clinical curative effect of the two treatment options.

NCT ID: NCT02592044 Recruiting - Pain Clinical Trials

Effect of Aromatherapy on Venopuncture Pain and Anxiety

Start date: November 2015
Phase: Phase 4
Study type: Interventional

The effect of aromatherapy with lavender essential oil on pain and anxiety during venipuncture will be evaluated.

NCT ID: NCT02570022 Recruiting - Pain Clinical Trials

Liposomal Bupivacaine in Total Shoulder Arthroplasty

EXP-TSA
Start date: October 2014
Phase: Phase 4
Study type: Interventional

This is a randomized, single blinded, standard of care controlled clinical trial. All adult patients over eighteen desiring shoulder arthroplasty will be eligible. The study compares pain control and opioid consumption in patients undergoing shoulder arthroplasty between patients receiving liposomal bupivacaine and those who underwent a preoperative inter-scalene nerve block.

NCT ID: NCT02563587 Recruiting - Pain Clinical Trials

Efficacy of Spontaneous Laughter in the Postoperative Treatment of Children

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

The purpose of this study is to determine the efficacy of laughter therapy in children to improve postoperative, evaluating the intensity of postoperative pain, anxiety and hospital stay.

NCT ID: NCT02510066 Recruiting - Pain Clinical Trials

Efficacy and Mechanisms of Acupuncture for Patients With Advanced Pancreatic Cancer Pain

Start date: July 2015
Phase: Phase 3
Study type: Interventional

This study compares the effect of acupuncture and placebo acupuncture on advanced pancreatic cancer pain and then investigates its potential mechanism of peripheral blood.

NCT ID: NCT02467140 Recruiting - Pain Clinical Trials

Comparing Pain After Laparoscopic Hernia Repair Using Two Different Types of Mesh Fixation

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

A clinical study evaluating acute and chronic pain following laparoscopic inguinal hernia repair comparing the ProGripTM self- fixating mesh with tack fixation.

NCT ID: NCT02454296 Recruiting - Pain Clinical Trials

Paracervical Block for Pain Associated With Laminaria Insertion

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

To assess if paracervical block is effective at reducing discomfort during placement of intracervical laminaria for pre-operative cervical preparation.

NCT ID: NCT02453945 Recruiting - Pain Clinical Trials

Use of a Support Bra to Reduce Pain and Improve Surgical Healing in Women Undergoing Sternotomy for Cardiac Surgery

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

The primary purpose of this study is to examine whether a properly fitted support bra on females improves their quality of life post-sternotomy. Specifically, does a support bra reduce discomfort, pain and wound dehiscence.

NCT ID: NCT02446262 Recruiting - Pain Clinical Trials

Neural and Psychological Mechanisms of Pain Perception

Start date: June 11, 2015
Phase: N/A
Study type: Interventional

Background: - Painful stimuli cause changes in a network of brain regions called the "Pain Matrix." But most of these regions respond to many other stimuli, not just pain. Researchers want to understand how different factors influence pain. They want to test what happens when people expect different levels of pain and receive treatments that can modify pain. They want to see if these factors influence decisions about pain and how the body responds to it. They also want to compare pain with responses like taste and vision. Objectives: - To better understand how pain and emotions are processed and influenced by psychological factors. Eligibility: - Healthy volunteers ages 18-50. Design: - This study requires 1 to 2 clinic visits that last 1 to 3 hours. - Participants will be screened with medical history and physical exam. - Some participants will have one or more magnetic resonance imaging (MRI) scans of their brain. For MRI, participants will lie on a table that slides in and out of a cylinder. The scanner makes loud knocking noises. They will get earplugs. - Participants heart activity will be recorded with electrocardiogram. Their pulse, sweating, and breathing will be monitored. - Some participants will take a taste test. Others may perform simple tasks. Others may receive pain in their arm, leg, or hand. The pain will come from heat or electric shocks. Others may judge pain using a topical pain-relieving cream. Some of these tests may be given during MRI. - Participants will fill out questionnaires. - The study will last 3 years.

NCT ID: NCT02440880 Recruiting - Pain Clinical Trials

Dexamethasone With TAP Block Increasing the Duration of the Peripheral Nerve Block in Caesarian Section

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

Nowadays Cesarean sections became the most popular surgery worldwide with the consumption of the hospital resources and the continuous need to decrease the costs, work load and medical stuff engagement. One of the most common problem is the need to control pain post operatively, this issue increase the work load over the pain management team and increase lead to patient in satisfaction. This study will test the usage of dexamethasone with different doses (4 and 8 mg) either locally or intravenously (I.V.) with the local anesthetics in TAP (transversus abdominis plane) block to prolong the duration of the block and decrease the need of post-operative analgesics.