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Discomfort clinical trials

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NCT ID: NCT06159569 Completed - Dry Eye Clinical Trials

Performance and Tolerability of the Medical Device LACRIACT

Start date: September 9, 2021
Phase: N/A
Study type: Interventional

The goal of this study is testing LACRIACT® eye drops, a medical device, to see how well it works and if people can use it safely. The Investigators will study this in people who have dry eyes, some of whom wear contact lenses, and some who do not. To obtain data from 20 participants, the investigators will first screen 22 patients, as two of them may not meet the requirements. If someone quits the study, the Investigators will not replace them with someone else. A person can partecipate in the study if they meet certain criteria in the study plan, complete the entire treatment, and use eye drops correctly at least 80% of the time. The Investigators running the study might also include up to 10 people who wear soft contact lenses out of the 20 in total. This study will be conducted at a clinic in Italy.

NCT ID: NCT06091046 Not yet recruiting - Critical Illness Clinical Trials

Discomfort in Intensive Care Patients - IPREA-N

Start date: August 2024
Phase:
Study type: Observational

The purpose of this study is to investigate discomforts experienced by intensive care patients during their critical illness period. We will use the Norwegian version of the questionnaire Inconforts des Patients de REAnimation (IPREA), the IPREA-N.Patients will be asked to rate18 questions about different possible discomforts on a 0-10 scale after their intensive care stay. Furthermore we aim to test whether the questionnaire when translated into Norwegian is useful in the Norwegian patient population. The aim of the study is - to assess perceived discomfort in intensive care patients using the IPREA-N questionnaire - to test psychometric properties of the questionnaire

NCT ID: NCT06053008 Recruiting - Pain Clinical Trials

The Relationship Between Pain Perception, Severity of Temporomandibular Joint Dysfunction, and Spinal Health in Geriatric Individuals

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

It is aimed to examine the relationship between pain perception, temporomandibular joint disorder severity and spine health in elderly individuals.

NCT ID: NCT06052735 Recruiting - Pain Clinical Trials

Association Among Pain Perception, Severity of Temporomandibular Joint Dysfunction, and Spinal Health in Caregivers of Stroke Individuals

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

This study aims to examine pain perception, temporomandibular disorder severity and spine health in caregivers of stroke patients.

NCT ID: NCT06037629 Recruiting - Acute Pain Clinical Trials

Premature Enhanced Automated Capture of Comfort Knowledge

PEACOCK
Start date: February 1, 2023
Phase:
Study type: Observational

The goal of this observational study is to develop methods that could provide continual monitoring of comfort levels for preterm neonates in hospitals.

NCT ID: NCT05731921 Completed - Empathy Clinical Trials

Effect of 'Empathy Dress' and Exercise on Midwifery Students' Discomfort, Empathy and Compassionate Love Levels

Start date: February 15, 2023
Phase: N/A
Study type: Interventional

To investigate the effect of the exercise program with the 'Empathy Dress' applied to midwifery students on the Levels of physical discomfort, empathy and compassionate love in the midwifery department of Amasya University. A total of 62 midwifery student are planned to be included in the study. Data will be collected with the "Student Information Form", "The Toronto Empathy Questionnaire- TEQ", "Evaluation Scale for Physical Discomfort", and "The Compassionate Love Scale". In the study, an exercise program that includes a total of eight sessions of 'Empathy Dress' and some exercises, every week and 20 minutes per week to the midwifery students in the experimental group, by the researcher. It is thought that the results of the study will improve the empathy and sensitive love levels of midwifery students and increase the quality of midwifery care offered.

NCT ID: NCT04381104 Recruiting - Pain Clinical Trials

Strategy to Cope Pain and Discomfort in Mammography

Start date: November 21, 2019
Phase: N/A
Study type: Interventional

Most of the women complain about the pain and discomfort during the mammography procedure. It is reported in the literature that most of the time these pain and discomfort are due to anxiety-related causes. During counseling before mammography scan, it was also observed that most of the women had a general belief that mammography is a very painful procedure and they have a negative perception about mammography. Thus, the Majority of pain seems due to anxiety-related issues. Studies also support this evidence and it is reported in the literature that most of the women avoid mammography scans due to this negative perception which causes delay and ultimately a late diagnosis. To validate the exact nature of pain and discomfort during mammography and to find out the strategy to cope with this anxiety-related pain and discomfort, there is a dire need for a study that can address this problem. Additionally, in our setup, most of the women who came for mammography are illiterate and belonged to the low socio-economic status. In these women, due to the negative perception, refusal or withdrawal rate is higher for mammography scans. A thorough literature search has revealed studies on this issue are scarce both nationally and internationally. In the current study, Paracetamol will be used as a possible intervention which is the safest premedication for reducing pain while achieving standard compression which is necessary for good image quality. Thus, this study can help develop a strategy to control mammography discontinuation due to pain and discomfort.

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: NCT03330483 Terminated - Pain Clinical Trials

Do Hydrophilic Catheters Decrease Pain and Discomfort of a Patient During Urodynamic Study

HYDRUDS
Start date: November 1, 2017
Phase:
Study type: Observational

This study attempts to verify whether different types of catheters could impact on patients' feelings at the first-time catheter insertion at urodynamic study. Each patient will undergo an insertion of only one type of a catheter and will rate his/her pain and discomfort feelings.

NCT ID: NCT03300999 Completed - Discomfort Clinical Trials

The Effects of Daily Ginger Tea Consumption in Reducing Discomfort During Menstruation

Start date: November 14, 2017
Phase: N/A
Study type: Interventional

The purpose of our graduate student research study is to observe the effect of drinking ginger tea daily on period discomfort.