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Pain clinical trials

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NCT ID: NCT04213716 Completed - Pain Clinical Trials

Comparison of the Efficacy of Calcium Hydroxide With Silver Nanoparticle and Conventional Calcium Hydroxide Intra Canal Medications on Post-Operative Pain in Symptomatic Root Canal Treatment Failure Cases:

CSNIMSRRT
Start date: June 15, 2015
Phase: Phase 2
Study type: Interventional

The aim of this study is to measure and compare the effectiveness of nanosilver combined calcium hydroxide and conventional calcium hydroxide intracanal medications in reducing postoperative pain in patients with Symptomatic Root Canal treatment Failure .

NCT ID: NCT04208659 Completed - Pain Clinical Trials

Veteran Ear Acupuncture Pilot Project

SAAAPP
Start date: February 27, 2020
Phase: N/A
Study type: Interventional

Veterans who have responded well to Battlefield Acupuncture (BFA), a form of auricular acupuncture, in routine clinical practice will be invited to receive education to insert the needles themselves at home. A 3D-printed wearable prosthetic will also be explored as a means to facilitate needle placement. Primary end-points will include whether adverse events occur over a six-month period and whether the aforementioned prosthesis significantly facilitates needle placement in terms of subjective ease of administration.

NCT ID: NCT04207710 Completed - Pain Clinical Trials

Safety of Gebauer's Pain Ease and Gebauer's Ethyl Chloride

Start date: January 26, 2021
Phase: Phase 4
Study type: Interventional

This study aims to determine if Gebauer's Pain Ease or Gebauer's Ethyl Chloride topical anesthetic sprays are safe for use as numbing agents prior to placing epidurals and arterial lines, based on whether they introduce increased microbial growth after application to skin. Due to the recent national shortage of lidocaine, we hope to find a suitable alternative to lidocaine for topical analgesia when placing arterial lines and epidurals. Our hypothesis is that the sprays will not affect the sterility of the area. We will compare microbial growth from three subsequent swabs taken from a single area of skin on the wrist and lower back: one with no treatment, the second after treatment with ChloraPrep, and the third after applying one of the numbing sprays. If there is significantly higher growth in the swabs containing the topical anesthetic spray versus the ChloraPrep alone, this will indicate that the sprays introduce microbes to the sites of skin.

NCT ID: NCT04202991 Completed - Pain Clinical Trials

The Relationship Between Pain, Balance and Gait in People With Chronic Obstructive Pulmonary Disease

Start date: May 1, 2019
Phase:
Study type: Observational

The balance, gait and pain in Chronic Obstructive Pulmonary Disease (COPD) study will aim to investigate the link between balance and gait impairment, and high rates of pain in people with COPD. This cross-sectional observational study will compare balance and gait outcomes for people with COPD who have pain, to those who are pain free.

NCT ID: NCT04185714 Completed - Pain Clinical Trials

THE EFFECTS OF KINESIO®TAPING IN PATIENTS WITH MIGRAINE

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

In patients with migraine, neck pain and trigger points in the neck muscles are common in clinical practice. This study was to investigate whether kinesiotaping applied to the cervical muscles has a clinical effect on pressure pain threshold, disability and quality of life in patients with migraine.

NCT ID: NCT04185233 Completed - Pain Clinical Trials

Distraction and Nitrous Oxide for Venous Puncture

DISPO
Start date: April 30, 2018
Phase: N/A
Study type: Interventional

This study will compare the efficiency of the iPad distraction or the administration of Nitrous Oxide on the anxiety decrease when a peripheral venous catheter is needed in children between 3 and 9 years old.

NCT ID: NCT04183049 Completed - Pain Clinical Trials

Improved Rehabilitation After Spinal Surgery in Adolescents

Start date: December 18, 2019
Phase:
Study type: Observational

Impact of the OFA technique on postoperative recovery from adolescent spine surgery and the incidence of chronic postoperative pain.

NCT ID: NCT04182191 Completed - Pain Clinical Trials

Influence of CYP2C9 Genotype on Clinical Efficacy of Tenoxicam

Start date: March 1, 2018
Phase: Phase 4
Study type: Interventional

The goal of this study is to evaluate the different gene haplotypes for the clinical efficacy of tenoxicam after third lower molar surgery for pain, edema and trismus, adverse reactions, need of rescue medication, patient satisfaction regarding the drug and the pharmacokinetics of the drug between the different gene haplotypes for CYP2C9 that are found in this population

NCT ID: NCT04177862 Completed - Pain Clinical Trials

Sublingual Sufentanil vs Intravenous Fentanyl for Acute Pain in the Ambulatory Surgery Center

Start date: December 11, 2019
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if a single dose of sublingual sufentanil is as or more efficacious than a single dose of IV fentanyl in a post anesthesia care setting.

NCT ID: NCT04176822 Completed - Pain Clinical Trials

Designing Animated Movie for Preoperative Period

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

Background: Using visual materials is effective in education to decrease children's pre-operative fear and post-operative pain. Children, especially those aged between 6 and 12 years, are interested in technology. This study aims to investigate the effects of watching an educational animated movie in the pre-operative period on fear and postoperative pain in children who are having surgery. Methods: The study was a prospective randomized controlled trial. This study was conducted between 6- to 12-year-old children in the Pediatric Surgery Clinic of Ege University Medical Faculty Hospital. The current study includes data from 132 children who were chosen doing block randomization. The "Child and Family Identification Data Form", "Children's Fear Scale" and "Wong-Baker FACES Pain Rating Scale" was used in data collection. The patients were divided randomly into three groups as the "Educational Animated Movie Group" (EAMG), "Documentary Movie Group" (DMG) and "Control Group" (CG). The Educational Animated Movie and Documentary Movie were screened using Virtual Reality (VR). Data were collected by the researcher in the pre-operative period. The pre-operative fear of the child was evaluated by the child and the parent, and the post-operative pain of the child was evaluated by the child, parent, and nurse using scales about fear and pain.