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NCT ID: NCT05549193 Completed - Clinical trials for Urinary Incontinence

The Effects of the Pelvic Floor and Abdominal Muscle Training on Urinary Incontinence

Start date: November 28, 2018
Phase: N/A
Study type: Interventional

To investigate the effects of the pelvic floor and abdominal muscle training on the severity of incontinence in women with stress and mixed urinary incontinence.

NCT ID: NCT05549063 Completed - Pes Planus Clinical Trials

Effect of Different Exercise Approaches on Balance and Proprioception in Individuals With Pes Planus

Start date: September 17, 2022
Phase: N/A
Study type: Interventional

Pes planus; It can be defined as the valgus of the hindfoot while loading the foot, the disappearance of the medial longitudinal arch in the midfoot, and the supination of the forefoot relative to the hindfoot. It may also occur due to the fact that the medial longitudinal arch in the foot is lower than the required height according to the anatomical position. The parts of the foot that touch the ground are anatomically healthy in a person; They are the heads of the calcaneus tuberositas calcanei on the back of the foot and the 5 metatarsal bones on the front of the foot. In the standing position, 25% of our body weight is on the tuber calcanei, while 25% is on the 5 metatarsal bones. In individuals with pes planus, convergence of the sole of the midfoot to the ground may even result in the sole of the midfoot touching the ground at its advanced levels. It is one of the common foot deformities.

NCT ID: NCT05549011 Completed - Hip Fractures Clinical Trials

PENG vs SIFI Block for Positioning Pain During Spinal Anesthesia

Start date: September 20, 2022
Phase:
Study type: Observational

This study aims to compare the effectiveness of preoperative ultrasound-guided suprainguinal fascia iliaca compartment block (SFICB) and pericapsular nerve group block (PENG) in preventing positioning pain during spinal anesthesia in patients who are scheduled for surgery due to hip fracture.

NCT ID: NCT05548998 Completed - Clinical trials for Neurocognitive Disorders

Effect of Low Flow Anesthetics on Neurocognitive Decline in the Elderly

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

This study aims to investigate the effect of inhaled anesthetics with a low fresh gas flow on cognitive function of elderly patients undergoing elective surgery

NCT ID: NCT05548790 Completed - Dental Anxiety Clinical Trials

Should Preoperative Information Before Impacted Third Molar Extraction?

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

The main objective of the present study was to evaluate the effects of different preoperative information techniques (verbal, written, video with background audio, and silent video with subtitles) on patients' anxiety levels before and after third molar extraction. The secondary objective was to determine the superiority of the information methods evaluated over each other. We hypothesized that the information provided by video with or without background audio would decrease preoperative and postoperative anxiety levels more effectively than information provided by verbal and written methods.

NCT ID: NCT05548751 Recruiting - Clinical trials for Lesch-Nyhan Syndrome

Physiotherapy Assessment Based on the ICF Model in The Lesch-Nyhan Syndrome: Case Report

Start date: September 26, 2022
Phase:
Study type: Observational

Lesch-Nyhan Syndrome (LNS) is a genetic disorder that results in a deficit in the hypoxanthine-guanine phosphoribosyltransferase (HPRT) enzyme, which affects purine metabolism. It is a genetic disorder that is carried by an X-linked recessive gene. LNS has 3 typical symptoms. These are increased uric acid, neurological symptoms and behavioral disorders. Dystonia is often seen among its neurological manifestations. Signs of primidal and extraprimidal system can be seen. It is very important to create the syndrome-specific physiotherapy program. In order to achieve this, evaluations based on the International Classification of Functioning, Disability and Health (ICF) model are valuable in terms of showing the right way in the management of the disease.

NCT ID: NCT05548673 Completed - Stress Clinical Trials

Evaluatıon of the Effıcıency of Stress Management Traınıng Applıed to Nursıng Students (Happy Nursıng Student)

Start date: July 24, 2020
Phase: N/A
Study type: Interventional

This research was conducted to determine the effect of stress management education on the perceived stress levels, coping styles, self-esteem, happiness and general health of nursing students. It was conducted in a mixed method as a randomized controlled intervention study.

NCT ID: NCT05548608 Completed - Clinical trials for Spinal Stenosis Lumbar

Lumbar Proprioception in Patients With Lumbar Spinal Stenosis

Start date: September 10, 2020
Phase:
Study type: Observational [Patient Registry]

The primary aim of this study was to compare spinal proprioception in patients with Lumbal Spinal Stenosis (LSS) (with or without surgery) and healthy controls. A secondary aim was to investigate the effect of pain at target positions where repositioning error (RE) was assessed and TLF flexibility on spinal proprioception deficiency.This cross-sectional and healthy controlled study was conducted in patients with LSS. Participants will be grouped as: Healthy control (Group I), chronic low back pain due to LSS (Group II) and undergoing surgery due to LSS (Group III). Reposition error (RE), pain at target positions of RE and flexibility of the TLF were assesed with iphone tiltmeter app, VAS and goniometric platform, respectively. Target positions of reposition error were: 30º forward bending and 15º backward bending in sitting and standing.

NCT ID: NCT05548361 Recruiting - Periodontitis Clinical Trials

The Use of Chlorhexidine and a Probiotic Lozenge in the Nonsurgical Therapy of Periodontitis

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

The aim of this study is determining the additional effect of a 2-week home usage of chlorhexidine in periodontitis patients undergoing scaling and root planing supplemented with a dual-strain probiotic lozenge.

NCT ID: NCT05548049 Completed - Clinical trials for Alveolar Bone Resorption

Autogenous Ramus Bone Block Harvesting With Piezosurgery

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

The aim of this randomized prospective clinical trial was to evaluate the outcome of bone block harvesting from the retromolar region using the Conventional and Piezosurgery Method. The study was planned on 19 patients (13F,6M) on 31 donor sites. In patients with bilateral bone harvesting, the donor site and the surgical method to be used were determined by the randomization protocol, while in patients with bone harvesting from a single site, the donor site was determined by considering parameters such as proximity to the operation site and distance to the inferior alveolar nerve. Clinical parameters such as operation time, pain, swelling, trismus, nerve damage were evaluated.