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Pain clinical trials

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NCT ID: NCT04526093 Recruiting - Depression Clinical Trials

Real-World Evidence in Patient-Reported Outcomes for Medical Cannabis (MC-RWE)

MC-RWE
Start date: July 15, 2020
Phase:
Study type: Observational

This prospective observational study aims to describe the effectiveness of MC on pain, epilepsy, sleep and /or anxiety/depression in a cohorts of patients authorized to use MC, using pre-defined, validated self assessment scales.

NCT ID: NCT04519931 Recruiting - Pain Clinical Trials

The Effect of Stress Ball Used During Endoscopy

Start date: November 5, 2020
Phase: N/A
Study type: Interventional

Endoscopy procedure is a frequently used method in the evaluation of the gastrointestinal system. Upper gastrointestinal system endoscopy can be performed with and without sedation. Sedation is the controlled sleep of the patient with certain drugs (pharmacological methods). Non-pharmacological methods help reduce anxiety and pain. In this study, a non-pharmacological stress ball will be used. It is aimed to evaluate the effect of using a stress ball on pain, anxiety and satisfaction during upper gastrointestinal system endoscopy.

NCT ID: NCT04519060 Recruiting - Pain Clinical Trials

Eye Shields for Infants After Dilated Exam

Start date: February 1, 2021
Phase: N/A
Study type: Interventional

The eyes of hospitalized infants are often assessed by dilated exam, and there is evidence that infants experience post-exam stress. Investigators will evaluate whether eye shields for infants after dilated eye exam lessen stress and discomfort.

NCT ID: NCT04512755 Recruiting - Pain Clinical Trials

AIMS Medical Outcomes Study

AMOS
Start date: July 1, 2020
Phase:
Study type: Observational

This epidemiologic research is being conducted as an observational prospective case series outcomes study of the use of advanced integrative specialty medical care and its effect on adult and pediatric patients with chronic or serious illnesses or mental health disorders.

NCT ID: NCT04503889 Recruiting - Pain Intensity Clinical Trials

The Effect of Transauricular Electrical Vagal Nerve Stimulation on Temporal Summation of Pain in Patients With Back Pain

TVNS_TSP_LBP
Start date: January 23, 2019
Phase: N/A
Study type: Interventional

The effect of transauricular electrical vagal nerve stimulation (taVNS) will be studied on temporal summation of heat pain (TSP) in 30 patients with chronic low-back pain and in 30 heathy volunteers. Participants will receive either taVNS or sham stimulation before and during TSP induction in a randomized crossover manner. The participants will be unaware regarding the type of intervention.

NCT ID: NCT04483141 Recruiting - Stroke Clinical Trials

Translation and Validation of the Abbey Pain Scale in Stroke Patients (ABBEY-F)

ABBEY-F
Start date: May 10, 2021
Phase:
Study type: Observational

Pain is common after a stroke, affecting up to 49% of patients within 2 years of the event. They include headache, musculoskeletal pain, spasticity and central neuropathic pain. A wide range of patients have communication problems after stroke that make it difficult to assess pain. Yet there is a major impact of pain on the quality of life of these patients. Some tools have been validated to assess pain in non-communicative patients, but none are specific to stroke patients. The Algoplus scale is commonly used in intra-hospital care in France. The Abbey Pain Scale is not translated into French, and could provide a more accurate pain rating for non-communicative patients. The objective is to validate a French version of the Abbey Pain Scale for stroke patients. It is an observational study with longitudinal data collection. It is planned to include 120 patients from the neurology department of the Clermont-Ferrand University Hospital.

NCT ID: NCT04467177 Recruiting - Pain Clinical Trials

Analgesic Effect of Oral Glucose in Neonates

Start date: July 1, 2020
Phase: N/A
Study type: Interventional

Background: Male circumcision is one of the oldest and most common operations performed all over the world. It can be performed at different ages, using different surgical techniques, for different religious, cultural and medical reasons. It was thought that the newborn baby does not experience pain because of incompletely developed nervous system. However, it has been shown that neurological system known to be associated with pain transmission and modulation, is intact and functional. OBJECTIVE: Our objective is to determine if a 30% glucose solution would reduce pain after circumcision compared with normal saline. STUDY DESIGN: This is a randomized placebo-controlled double-blinded clinical trial. POPULATION: We will include full term neonates, who will be recruited from the inpatient nursery at Makassed General Hospital over a 1-year period. OUTCOME MEASURE: The primary outcome is to assess efficacy of 30% glucose on pain measured using the Neonatal Infant Pain Score. Secondary outcome is to assess effect of 30% glucose oh physiologic parameters

NCT ID: NCT04461470 Recruiting - Pain Clinical Trials

6-Month Outcomes of PEMF to Nucleotide Sources Revealing Cell Sensory Experience in Pain Relief, Stress Relief and Anti Ageing Restoration

PEMF
Start date: August 29, 2019
Phase:
Study type: Observational [Patient Registry]

Background: The hz Clinic registry is a programme made of five scheduled cohorts designed to include participants dealing with Immunity compromise, Pain, Ageing and Stress (general and pandemic anxieties) who are to be followed for 6 month to five years in their structured routine of pulsed electro resonance (PEMF) to determine their clinical outcome in the real world, contributing evidence for benchmarking fellow cohort participant variance. Here we report baseline characteristics, PEMF transfer events and outcomes in participants in the UK. This study serves as a calibration proforma for downstream real world evidence observations of PEMF in the field.

NCT ID: NCT04451863 Recruiting - Pain Clinical Trials

Analgesic and Subjective Effects of Terpenes

Start date: December 15, 2021
Phase: Phase 1
Study type: Interventional

The purpose of this research is to assess the analgesic and subjective effects of terpenes administered alone and in combination of THC.

NCT ID: NCT04429282 Recruiting - Pain Clinical Trials

A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial of Intravenous Ibuprofen 400 and 800 mg Every 6 Hours in the Management of Postoperative Pain.

Start date: June 10, 2020
Phase: Phase 3
Study type: Interventional

This study was to evaluate the efficacy and safety of intravenously administered ibuprofen 400mg and 800 mg q6h for the management of moderate to severe postoperative pain in Chinese population.