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Acute Pain clinical trials

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NCT ID: NCT03305055 Terminated - Clinical trials for Posttraumatic Stress Disorder

RCT: Fentanyl Plus Ketamine Versus Fentanyl Alone for Acute Burn Pain

Start date: December 16, 2017
Phase: Phase 4
Study type: Interventional

The Ketamine for Acute Pain in Burns study is a randomized, double-blind, parallel group trial (RCT) with active control (usual care) contrasting the efficacy and safety of "Ketamine Plus Opiate-based usual care" (O+K) with the safety and efficacy of the "Current Standard of Care". THe current standard of care is an opiate medication alone, Fentanyl (Usual Care-Opiate (UC-O), dose/timing as per Burn Center protocol).

NCT ID: NCT03224975 Terminated - Clinical trials for Magnetic Resonance Imaging

Acute Pain Memory Among Former Burned: Exploration of fMRI.

EXPLO-DMA
Start date: February 13, 2018
Phase: N/A
Study type: Interventional

Pain is complex phenomenon misunderstood in spite of medical progress and neurosciences. That's why the relief of chronic pain is only partial for a lot of infection as arthrosis, chronic back pain, headaches or neuropathic pain. Certain situations bring to relive pain sensation. Investigators were interested to former burned. They wonder about somatic memory and unconscious of acute.

NCT ID: NCT03206216 Terminated - Pain, Acute Clinical Trials

Feasibility Study of New Method of Diagnostic and Prediction of Painful CIPN

Start date: August 4, 2017
Phase: N/A
Study type: Interventional

This clinical trial studies how well Diode laser fiber type Selective Stimulator (DLss) works in predicting pain development in patients with ovarian cancer who are receiving chemotherapy. Stimulating of the pain nerve fibers in the skin with laser light stimulation may help to predict whether a patient will develop painful peripheral neuropathy, correlate with the severity of neuropathy during and after chemotherapy treatment, and may help to explain the mechanisms of chemotherapy-induced neuropathic pain (CIPN).

NCT ID: NCT03157882 Terminated - Pain Clinical Trials

Pediatric Pain Assessment in the Emergency Department

Start date: August 13, 2016
Phase:
Study type: Observational

To examine pediatric pain assessment in the Emergency Department

NCT ID: NCT03127592 Terminated - Pain, Acute Clinical Trials

Phase III Efficacy and Tolerability Trial of the Fixed Dose Combination of Etodolac 400 mg and Cyclobenzaprine 10 mg Versus Isolated Active Substances in Pain Control After Impacted Third Molar Extraction

FDCETCB-III
Start date: October 5, 2020
Phase: Phase 3
Study type: Interventional

This Phase III study will compare the efficacy and tolerability of a Fixed Dose Combination of Etodolac + Cyclobenzaprine versus the isolated drugs in postoperative pain control after impacted third molar extraction.

NCT ID: NCT03063359 Terminated - Pain, Acute Clinical Trials

Intranasal Fentanyl Versus Oral Morphine Sulfate in the Treatment of Pain in Pediatric Trauma

FINDOL
Start date: May 30, 2017
Phase: Phase 3
Study type: Interventional

Acute tramatic pain is one of main reasons for consultation in pediatric emergency departments. To manage pain quickly and effectively must be a primary outcome of the emergency department. However, pediatric emergency department are sometimes criticized for inadequate and delayed initiation analgesia . Indeed, several studies have shown the inadequacy between the intensity of the pain evaluated by the care team and the therapeutic management of it. The ideal analgesic must have a rapid onset of action, have a powerful analgesic effect, have few side effects and can be administered quickly and painlessly. That's why, the main outcome of this study is to assess the non inferiority of a treatment by intranasal Fentanyl vs morphine sulfate (oral use) in children with traumatic pain on arrival to pediatric emergency department.

NCT ID: NCT02846610 Terminated - Pain, Postoperative Clinical Trials

Registry for Acute Pain Treatment

Start date: September 2007
Phase:
Study type: Observational [Patient Registry]

The German Network for acute pain management and Regional Anesthesia (NRA) is a multi-center, non-interventional registry and benchmark project, assessing and analysing clinical and patient-reported procedural and outcome data of systemic analgesia and regional anesthesia hosted by the German Society of Anesthesia and Intensive Care Medicine (DGAI) and professional Society German Anesthetists (BDA)

NCT ID: NCT02773472 Terminated - Acute Pain Clinical Trials

Electroacupuncture for Laparoscopic/ Robotic Colorectal Surgery

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

A multimodal approach for management of post-operative pain is used to improve analgesia, minimize side effects, and improve recovery. Nevertheless, opioid analgesics and intravenous patient controlled analgesia remains the mainstay of postoperative analgesia after colorectal surgery. Opioids are associated with various side effects such as nausea, vomiting, sedation, dizziness, respiratory depression, urinary retention and reduced bowel movement. These side effects are unpleasant and lead to prolonged recovery. Use of non-pharmacological analgesic techniques may improve postoperative pain control and reduce opioid consumption. Acupuncture has been used for over 3000 years in China for treatment of pain and various other conditions. Acupuncture and related techniques are simple and safe. There is evidence that acupuncture can reduce postoperative pain intensity, opioid consumption, and opioid related side effects.

NCT ID: NCT02746263 Terminated - Clinical trials for Acute Pain, Postoperative

Multicenter Study to Compare Intravenous and Oral Acetaminophen for the Treatment of Acute Moderate to Severe Pain

Start date: April 27, 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare intravenous (IV) and oral acetaminophen for the treatment of acute moderate to severe pain in combination with standard patient-controlled analgesia (PCA) in adult subjects following total knee replacement.

NCT ID: NCT02729207 Terminated - Ankle Sprain Clinical Trials

Proof-of-concept Study of NSAID Hydrogel Patch in Treatment of Acute Pain

Start date: July 2016
Phase: Phase 2
Study type: Interventional

The safety and the efficacy of the Esflurbiprofen Hydrogel Patch will be assessed in comparing with placebo in the treatment of acute pain due to ankle sprain