Clinical Trials Logo

Pain, Acute clinical trials

View clinical trials related to Pain, Acute.

Filter by:

NCT ID: NCT05834023 Completed - Postoperative Pain Clinical Trials

Bupivacaine Versus Bupivacaine Plus Lidocaine in Infraclavicular Block

Start date: May 2, 2023
Phase: Phase 4
Study type: Interventional

In this study, the investigators will compare two different anesthetic solutions in the infraclavicular block in patients having forearm, wrist, and hand surgery. The solutions will be bupivacaine 0.5% versus bupivacaine 0.25% plus lidocaine 1%, both associated with epinephrine 5 mcg/ml and dexamethasone 4 mg. The main objective of this investigation is to demonstrate that using higher concentrations of bupivacaine alone results in a significant block duration increase compared with the mixture of bupivacaine and lidocaine.

NCT ID: NCT05828264 Completed - Pain, Acute Clinical Trials

The Effect of "Quantum-Touch" on Pain, Fear, and Anxiety of the Children

Start date: September 1, 2022
Phase: N/A
Study type: Interventional

This research is a randomized controlled experimental study designed to determine the effect of the Quantum-Touch method applied during the vascular access procedure in children aged 7-12 years, on the level of pain, fear and anxiety in children.

NCT ID: NCT05818761 Completed - Pain, Acute Clinical Trials

Distraction on Procedure-Related Emotional Appearance, Pain, Fear, and Anxiety During Phlebotomy in Children

VR-DEU22
Start date: November 1, 2022
Phase: N/A
Study type: Interventional

This randomized controlled study was planned to evaluate the effects of distraction methods, using virtual reality or a stress ball, on the emotional appearance, pain, fear, and anxiety associated with the procedure, during the phlebotomy in children aged 6-12 in a private blood collection unit.

NCT ID: NCT05781230 Completed - Knee Osteoarthritis Clinical Trials

The Effect of Exercises of Different Intensity Applied After Total Knee Arthroplasty on Exercise-Induced Hypoalgesia

Start date: January 1, 2022
Phase: N/A
Study type: Interventional

The aim of this study was to investigate whether exercise-induced hypoalgesia (EIH) is present following exercise in patient after total knee arthroplasty (TKA) and if so, if it changes with exercise intensity. A repeated measures and single-blinded randomized study were done. Thirty-eight patients 24 hours after TKA were randomly assigned to either low intensity exercises (LIE) group or high intensity exercises (HIE) group. An exercise programs lasted for five days during the hospitalization period. Pain severity was assessed by Visual Analog Scale (VAS) (0-10 mm). Pressure pain thresholds (PPTs) were measured over quadriceps and biceps brachii and muscles immediately before and after exercise.

NCT ID: NCT05744544 Completed - Pain Clinical Trials

Sensory Assessment and Regression Rate of Bilateral External Oblique Intercostal Block and m-TAPA Block

Start date: May 2, 2023
Phase:
Study type: Observational [Patient Registry]

External oblique and m-tapa blocks are routinely performed on patients undergoing laparoscopic cholecystectomy in our clinic. In this study, sensory block and regression rates will be investigated in patients who underwent block.

NCT ID: NCT05679453 Completed - Pain, Acute Clinical Trials

Lornoxicam Versus Etodolac After Third Molar Surgery

Start date: July 20, 2022
Phase: Phase 4
Study type: Interventional

Our study aimed to compare the effect of lornoxicam and etodolac on postoperative pain, edema and trismus following lower third molar extraction

NCT ID: NCT05675358 Completed - Pain, Acute Clinical Trials

Virtual Reality on Pain, Fear, and Emotional Appearance During Phlebotomy in Pediatric Hematology and Oncology Patients

VR-PHO
Start date: March 3, 2022
Phase: N/A
Study type: Interventional

In this study, the effect of virtual reality, which is one of the pain relief methods, on the pain, fear and emotional appearance associated with the procedure, was evaluated in children aged 4-12 years who will undergo phelobotomy in a Pediatric Hematology and Oncology outpatient clinic.

NCT ID: NCT05625776 Completed - Pain, Acute Clinical Trials

Effects of Acute Pain on Cognitive Performance in Young Adults

Start date: March 22, 2023
Phase: N/A
Study type: Interventional

The effects of pain on cognitive performance have not been thoroughly investigated. Broadly, the purpose of this research is to investigate the effects of acute pain on performance of a variety of cognitive performance measures. The investigators hypothesize that acute pain impairs cognitive performance, particularly cognitive measures of working memory, attention, and processing speed.

NCT ID: NCT05577832 Completed - Pain, Acute Clinical Trials

Testing Different Methods of Intramuscular Injection

Start date: May 1, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to compare in different injection techniques. The main question[s] it aims to answer are: - Is there a difference between the pain levels due to needle insertion in the injection made with the HST Technique, the ShotBlocker technique and the standard technique? - Is there a difference between the hematoma levels of the injection made with the HST Technique, the ShotBlocker technique and the standard technique? - Is there a difference between the comfort levels of the injection made with the HST Technique, ShotBlocker technique and standard technique? - Is there a difference between the satisfaction levels of the patients with the injection made with the HST Technique, ShotBlocker technique and standard technique? - Is there a difference between the injection fear levels of patients with HST Technique, ShotBlocker technique and standard technique?

NCT ID: NCT05563233 Completed - Pain, Acute Clinical Trials

ShotBloker and Helfer Skin Tap Technique During Intramuscular Injection in Children

Start date: April 10, 2022
Phase: N/A
Study type: Interventional

To examine the effect of the Helfer skin tap technique and ShotBloker application on pain and fear experienced during intramuscular injection in children aged 6-12 in the pediatric emergency unit. It was planned as a randomized controlled experimental study to determine its effect on fear. The population of the study will be children aged 6-12 years who applied to the Tarsus State Hospital, and Pediatric Emergency Clinic and the sample will be 177 children who will undergo intramuscular intervention and meet the criteria for inclusion in the study. In data collection; Data collection form, Wong-Baker Scale, and Child fear scale will be used. In order to examine the mean scores of pain and fear according to intramuscular administration techniques in children, appropriate tests will be used by making an analysis of conformity to normal distribution.