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NCT ID: NCT05176431 Completed - Coccyx Disorder Clinical Trials

Radial and Focused ESWT in the Treatment of Coccydynia According to Age and Body Mass Index

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

To date, focused and radial types of ESWT have been effectively used in the treatment of coccydynia. However, studies directly addressing a comparison between radial and focused types of ESWT in coccydynia have not been done. Therefore, this study aims to evaluate comparative effects of radial and focused ESWT options on coccydynia.

NCT ID: NCT05176028 Completed - Clinical trials for Arthroscopic Rotator Cuff Repair

Acute Effects of Fascial Release Technique in Patients With Rotator Cuff Repair

Start date: January 3, 2018
Phase: N/A
Study type: Interventional

This study was planned to investigate the acute effects of fascia technique on pain, range of motion, upper extremity functional level, and kinesiophobia in individuals with arthroscopic rotator cuff repair.Thirty volunteers with an arthroscopic rotator cuff repair were included to study. The individuals were randomly divided into two groups. While hot pack, interferential current and exercise program were applied to the classical physiotherapy group, the fascial release technique was applied to the treatment group in addition to the classical physiotherapy program for 2 weeks with 2 sessions per week. Individuals were assessed for pain severity by using Visual Analog Scale, range of motion by goniometer, functional level by SPADI, kinesiophobia by Tampa Kinesiophobia Scale before and after treatment and satisfaction level by using Visual Analogue Scale after treatment.

NCT ID: NCT05175924 Completed - Children, Only Clinical Trials

The Effect of Virtual Reality On Pain and Anxiety During Blood Draw in Children: A Randomized Controlled Study

Start date: May 15, 2021
Phase: N/A
Study type: Interventional

Purpose: The study was carried out to determine the effect of virtual reality applied during blood collection upon pain and anxiety in children aged 5-12. Design and Methods: In this randomized controlled study, children included in the sample group were assigned to the control group (n=43) and Aquarium VR group (n=45) using block randomization. "Child State Anxiety Scale " and "Wong-Baker Faces Pain Scale" were used to collect the data of the study. Children in the Aquarium VR group watched the "Aquarium VR" application through virtual reality glasses during the procedure. The children in the control group benefited from routine nursing services. The pain scores after blood collection and anxiety scores before and during blood collection in children in both groups were interpreted.

NCT ID: NCT05175872 Completed - Trauma Injury Clinical Trials

Factors Affecting Mortality and Morbidity in Trauma Patients Followed in Intensive Care Unit

trauma
Start date: October 14, 2019
Phase:
Study type: Observational

In this study, the demographic and clinical characteristics of trauma patients followed up in the Intensive Care Unit of the Anesthesiology and Reanimation Clinic of the Health Sciences University Okmeydanı Training and Research Hospital for a 2-year period were evaluated prospectively to determine the morbidity and mortality rates and to determine the factors affecting these rates. data.

NCT ID: NCT05175820 Completed - COVID-19 Clinical Trials

COVID-19 and Working Conditions of Dentists

Start date: September 21, 2020
Phase:
Study type: Observational

The aim of this study is to evaluate the protective measures and awareness of dentists working in Turkey regarding the COVID-19 pandemic.

NCT ID: NCT05175729 Completed - Pregnancy Related Clinical Trials

Comparing Anterior Segment Parameters During Pregnancy and Post-Pregnancy

Start date: December 1, 2021
Phase:
Study type: Observational

The aim of this study is to evaluate anterior segment changes during and after pregnancy, and compare them with non pregnant healty women

NCT ID: NCT05175482 Completed - Health Behavior Clinical Trials

Health Belief Model Based Education on Human Papilloma Virus Infection and Vaccination

Start date: December 30, 2021
Phase: N/A
Study type: Interventional

To evaluate impact of Health Belief Model Based Education on Human Papilloma Virus Infection and Vaccination among University Students

NCT ID: NCT05175209 Completed - Ulnar Neuropathies Clinical Trials

The Effect of Ulnar Nerve Entrapment Localization on Ipsilateral Upper Extremity Functions. The Effect of Ulnar Nerve Entrapment Localization on Ipsilateral Upper Extremity Functions. The Effect of Ulnar Nerve Entrapment Localization on Ipsilateral Upper Extremity Functions.

Start date: January 19, 2022
Phase: N/A
Study type: Interventional

Regardless of the cause of ulnar nerve entrapment neuropathy, investigators are planning to explore the relationship between the ipsilateral upper extremity dysfunction that may develop due to ulnar neuropathy and the level of entrapment in electromyelography.

NCT ID: NCT05175027 Completed - Circumcision Clinical Trials

Preoperative Antiseptic in Newborn Circumcision Comparison of Povidone Iodine and Hypochlorous Acid Used

Start date: May 5, 2021
Phase: N/A
Study type: Interventional

Comparison of Povidone iodine and Hypochlorous acid used as a Preoperative Antiseptic in Newborn Circumcision abstract Aim: Circumcision is one of the most common surgical procedures in all age groups. Before the circumcision procedure, asepsis is provided with a surface disinfectant. Various methods can be used for this process. Povidone iodine, which has been used for years during the transition from traditional circumcision methods to surgical circumcision methods; tissue damage, allergic reactions and increase in pain level. For this reason, the investigators aimed to compare it with Hypochlorous acid (Crystalin), which is a less toxic and more physiological antiseptic solution. Material and Method: Newborns to be circumcised randomly were divided into two groups as Hypochlorosis group and Povidone iodine group. At the beginning of the circumcision procedure, a culture was taken in the form of a prepucial swab 1 minute after the cleaning of the local area and the inner surface of the prepuce. Then circumcision was performed. Culture results and complications were compared.

NCT ID: NCT05174897 Recruiting - Pain Clinical Trials

The Effect of Emotional Freedom Technique on Fear and Pain in Intravenous Catheter Applications in Pediatric Emergency

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

This study was planned to determine the effect of emotional liberation technique (EFT) in reducing fear and pain in intravenous catheter applications in children aged 10-14 years admitted to the pediatric emergency department.