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Pain clinical trials

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NCT ID: NCT02107456 Completed - Pain Clinical Trials

Effect of Dry Needling on Myofascial Trigger Point

Start date: July 2012
Phase: N/A
Study type: Interventional

Myofascial trigger point is one of the most common causes of musculoskeletal disorders. Myofascial trigger point in upper trapezius has been reported as a symptom in patients with neck and upper thoracic pain. The purpose of this study was to investigate the prolonged effect of dry needling on myofascial trigger point in upper trapezius muscle.

NCT ID: NCT02104050 Completed - Pain Clinical Trials

Study of OLT1177 Gel to Treat Moderate to Severe OA Knee Pain

Start date: April 2014
Phase: Phase 2
Study type: Interventional

The objectives of this trial are to investigate the efficacy and safety of six weeks of treatment with OLT1177 Gel in subjects with moderate to severe pain associated with osteoarthritis of the knee following cessation of pain therapy.

NCT ID: NCT02102516 Completed - Pain Clinical Trials

SPRIX in 0 to 11 Year-Old Patients Undergoing Open Surgical Procedures

Start date: March 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the pharmacokinetics and safety of postoperative administration of SPRIX in pediatric patients (ages 0-11) undergoing open surgical procedures.

NCT ID: NCT02102178 Completed - Pain Clinical Trials

Occupational Therapy Modulates the Pain in Cancer Patient Under Palliative Care

Start date: July 2007
Phase: Phase 2
Study type: Interventional

Pain is one of the most incapacitating symptoms because it is a complex experience that includes sensory and emotional perceptions, in which sensory, affective, cognitive, behavioral, cultural and social characteristics interact. Around 79% of advanced cancer cases present pain. There is evidence that non-pharmacological therapeutic activities are useful for controlling oncological pain and other symptoms resulting from such diseases. This study evaluated the results relating to pain modulation and improvement of emotional symptoms and quality of life, from an occupational therapy program applied to oncological patients who were receiving palliative care.

NCT ID: NCT02100670 Completed - Pain Clinical Trials

A Multicenter Efficacy Study of a Diclofenac+Menthol Gel in Subjects With Ankle Sprain

Start date: November 1, 2013
Phase: Phase 3
Study type: Interventional

This Phase III pivotal efficacy study will assess efficacy and onset of pain relief of MFC51123 gel vs. placebo and MFC51123 gel vs. 1% diclofenac gel and 3% menthol gel in participants with an ankle sprain to support topical MFC51123 gel registration.

NCT ID: NCT02096003 Completed - Pain Clinical Trials

Intrathecal Hydromorphone for Pain Control After Cesarean Section

Start date: May 2014
Phase: Phase 2
Study type: Interventional

The use of intrathecal opioids for analgesia in the setting of cesarean section has become standard obstetric anesthesia practice. Currently, two opioids are commonly used. These opioids are fentanyl and morphine (Duramorph). Intrathecal opioids are an excellent source of analgesia and act to reduce the stress response to surgery. Currently, most obstetric anesthesiologists use intrathecal morphine for analgesia after cesarean delivery. Morphine provides excellent analgesia for cesarean section. However, use of this medication is associated with side effects such as pruritus and nausea and vomiting. Recently, multiple obstetric anesthesia groups began to use intrathecal hydromorphone for cesarean delivery when morphine was unavailable. As groups began to use hydromorphone, retrospective data became available that demonstrated its safety and efficacy for use during cesarean section. In order to fully elucidate the analgesic and side effect properties of hydromorphone for cesarean delivery, a prospective randomized, double blind study comparing morphine and hydromorphone is necessary. The investigators need to understand whether hydromorphone is as effective as morphine for analgesia after cesarean section, and whether it is associated with fewer or more side effects. The results of the study will allow providers to make educated decisions to better care for their patient.

NCT ID: NCT02093637 Completed - Pain Clinical Trials

Rapid Extremity Pain Relief by Battlefield Acupuncture After Orthopedic Surgery

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

The purpose of this study is to determine if the addition of Battlefield Auricular Acupuncture (BFA) to standard therapy causes reduction in pain, medication use, time to ambulation without assistance, hours missed from work and increases quality of life after lower extremity surgery at two Air Force Medical Centers.

NCT ID: NCT02092454 Completed - Pain Clinical Trials

Study to Assess the Safety and Efficacy of Benzocaine for Pain Relief in Children Presenting With Acute Otitis Media

Start date: September 2013
Phase: Phase 2
Study type: Interventional

To assess the clinical safety and efficacy of the Benzocaine relative to placebo in pain relief associated with acute otitis media.

NCT ID: NCT02089581 Completed - Pain Clinical Trials

A Study of Whether 2 New Oral Formulations of a Strong Pain Killer Release the Same Amount of Drug Into the Body as the Marketed Medication

Start date: April 2014
Phase: Phase 1
Study type: Interventional

To determine whether two new oral formulations of a strong pain killer release the drug into the body in a similar pattern as the already marketed reference capsule formulation with or without food.

NCT ID: NCT02087748 Completed - Pain Clinical Trials

An Investigator Initiated, Within-Subject, Proof of Concept Study to Assess the Efficacy and Safety of Voltaren Gel in Subjects With DOMS

Start date: March 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate analgesic efficacy of Topical Voltaren Gel (diclofenac sodium gel) 1% applied QID compared to Placebo in Subjects Experiencing Delayed Onset Muscle Soreness.