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Pain clinical trials

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NCT ID: NCT01814397 Completed - Breast Cancer Clinical Trials

Pilot Study to Evaluate the Effect of Aromatase Inhibitor Therapy on Pain Threshold in Breast Cancer Patients

Start date: July 2009
Phase:
Study type: Observational

Postmenopausal women who have hormone receptor positive breast cancer are typically treated with aromatase inhibitor medications, which substantially decrease the amount of estrogen produced by their bodies. These medications are fairly well tolerated, but can cause aches and pains which can be quite severe in some cases. People experience pain differently. Estrogen appears to play a role in how we experience pain. Therefore, decreasing estrogen levels may lead to more pain in some women than others. The goal of this study is to evaluate perception of pain in women with breast cancer, and to determine if differences in pain perception lead to more aches and pains in some women treated with aromatase inhibitors. In this study, we plan to enroll 55 women with breast cancer who are starting treatment with an aromatase inhibitor. Participants will undergo testing to evaluate their perception of pain, and will also complete a set of questionnaires. Testing will be conducted before starting aromatase inhibitor therapy, as well as after 3 and 6 months of therapy. We will investigate whether pre-existing differences in pain perception lead to different amounts of pain during aromatase inhibitor therapy.

NCT ID: NCT01813695 Completed - Pain Clinical Trials

Preemptive Genotyping and Pain Management

Start date: March 2013
Phase:
Study type: Observational

The purpose of this study is to see if testing for genes related to pain and pain management before surgery affects how patients are treated for pain after surgery. The investigators want to know if this information will be used to effectively treat patients for pain after surgery if the clinical staff have a chance to review it before the surgery.

NCT ID: NCT01812928 Completed - Pain Clinical Trials

Diclofenac Suppository to Control Pain During Flexible Cystoscopy

DUF
Start date: March 2013
Phase: Phase 2
Study type: Interventional

Flexible cystoscopy has diagnostic as well as therapeutic role in many patients presenting in urology clinic with lower urinary tract symptoms (frequency, nocturia etc) and hematuria (blood in urine). Pain associated with cystoscopy varies from patient to patient, majority requires local anesthesia or lubricant solution only. During flexible cystoscopy, lubrication, use of topical anesthesia and duration of cystoscopy are recognized as important factors contributing in severity of pain of which use of intraurethral gel left to individual preference. Various studies are available reporting the pain perception with use of various intraurethral gels. Even the highest level of evidence is unable to resolve the query. With this study the investigators hypothesize that pain perception (recorded in form of pain score) during flexible cystoscopy can be reduced with use of per operative diclofenac(Non Steroidal Anti Inflammatory Drug)suppository in comparison to plain gel alone. With better control of pain the investigators aim to increase patient comfort and compliance which will increase the patient satisfaction rate and early return to work.

NCT ID: NCT01812733 Completed - Pain Clinical Trials

Non-interventional Study Comparing Targiniq and Oxycodone/Laxatives

Start date: June 2013
Phase: N/A
Study type: Observational

The objective of the non-interventional study is to compare the quality of life, health care resource use and costs between the use of a combination of oxycodone and naloxone (Targiniq) versus oxycodone and laxatives for patients with severe pain, and to evaluate the cost-effectiveness of treatment with Targiniq.

NCT ID: NCT01805661 Completed - Pain Clinical Trials

Adductor Canal Block With Posterior Capsular Injection for Total Knee Replacement

Start date: March 2013
Phase: N/A
Study type: Interventional

To compare early ambulation and ability to participate in rehabilitation in patients undergoing total knee replacement using two different nerve block techniques for pain control. The 2 methods are 1) Adductor canal block with posterior capsular injection 2) femoral nerve block with tibial nerve block

NCT ID: NCT01803529 Completed - Pain Clinical Trials

Deep Friction Massage for Intercostal Pain in Patients With Heart Disease

Start date: October 2003
Phase: N/A
Study type: Interventional

Studies show that chest pain is a common complaint presented in both general practice and in emergency units. Musculoskeletal causes are common, but frequently overlooked. No studies about treatment of chest pain from the intercostal muscles were found by search in medical literature databases. The purpose of this study is to evaluate the effect of two different physical therapy interventions on intercostal pain in patients with stable heart disease. The hypothesis was that deep friction massage combined with heat-pack is more effective than heat-pack only.

NCT ID: NCT01802086 Completed - Pain Clinical Trials

Emla-Cream as Pain Relief During Pneumococcal Vaccination

Start date: May 2013
Phase: N/A
Study type: Interventional

The aim of this intervention study is to compare the efficacy of Emla cream as a pain relief or no pain relief in connection to the first pneumococcal vaccination at the age of three months in Child health care. Primary objective 1.Leads Emla cream as pain relief to children in connection with pneumococcal vaccination at the age of three months to lower pain scores in the use of FLACC as a pain measurement instrument?

NCT ID: NCT01800318 Completed - Pain Clinical Trials

Does Noninvasive Electrical Stimulation of Acupuncture Points (NESAP) Reduce Heelstick Pain in Infants?

Start date: March 2013
Phase: N/A
Study type: Interventional

The purpose of the study is to determine whether noninvasive electrical stimulation at acupuncture points (NESAP) and/or 24% sucrose is effective in reducing pain in infants during invasive procedures. The investigators hypothesize that: - Gentle noninvasive electrical stimulation at selected acupuncture points and/or oral use of 24% sucrose with pacifier will reduce the newborn infant's responses to heelstick pain, as measured by the Premature Infant Pain Profile (PIPP), heart rate variability, duration of crying, and salivary cortisol levels. - The effects of combined therapies will be additive. - The analgesic effects of NESAP and/or sucrose will continue for the duration of the heelstick, reflected by the first two minutes of heelstick and the first two minutes of recovery.

NCT ID: NCT01795157 Completed - Pain Clinical Trials

Computer Based Assessment and Treatment

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

This study aims to investigate computer based symptom assessment in an outpatient cancer population, and the use of a computer based decision support system to facilitate the diagnosis and treatment of cancer related pain. Primary hypothesis is, that this approach improves pain control and pain management in an unselected group of cancer patients in an outpatient setting. - Improvement of average pain last 24 hours by at least 1.5 points on a 0-11 scale - Improvement of worst pain last 24 hours by at least 1.5 points on a 0-11 scale - An alteration in the prescribing dose of opioids in equipotent opioid dosage Secondary hypothesis is, that this system improves overall symptom control and symptom management in an unselected group of cancer patients in an outpatient setting.

NCT ID: NCT01794923 Completed - Pain Clinical Trials

Topical Ibuprofen for Delayed Onset Mulscle Soreness

Start date: June 13, 2013
Phase: Phase 3
Study type: Interventional

The objective of this study is to compare the efficacy and safety of Ibuprofen 5% Topical Gel versus placebo administered two or three times daily for the treatment of pain associated with delayed onset muscle soreness following intense eccentric exercise of the elbow flexor muscles.