Clinical Trials Logo

Filter by:
NCT ID: NCT04519931 Recruiting - Pain Clinical Trials

The Effect of Stress Ball Used During Endoscopy

Start date: November 5, 2020
Phase: N/A
Study type: Interventional

Endoscopy procedure is a frequently used method in the evaluation of the gastrointestinal system. Upper gastrointestinal system endoscopy can be performed with and without sedation. Sedation is the controlled sleep of the patient with certain drugs (pharmacological methods). Non-pharmacological methods help reduce anxiety and pain. In this study, a non-pharmacological stress ball will be used. It is aimed to evaluate the effect of using a stress ball on pain, anxiety and satisfaction during upper gastrointestinal system endoscopy.

NCT ID: NCT04519346 Completed - Migraine Headache Clinical Trials

Mesotherapy Versus Systemic Therapyin Treatment of Migraine Headache

Start date: December 1, 2019
Phase: N/A
Study type: Interventional

Introduction:Migraine is a prevalent disabling primary headache disorder which is classified in two major types; migraine without aura and migraine with aura. The aim of this study was to compare the efficiency of mesotherapy with systemic therapy in pain controlin patients with headache related tomigraine without aura. Methods: We conducted this prospective parallel randomized controlled trial with the patients admitted to the emergency department with headache related to migraine without aura. One group was treated with mesotherapy, and the control group with intravenous dexketoprofen. Changes in pain intensity at 30th minute, 60th minute, 120th minute and 24th hours after treatment using Visual Analogue Scale (VAS), need to use analgesic drug within 24 hours,re-admission with same complaint to emergency department (ED) within 72 hours, and adverse effect rate of the methods were compared between groups.

NCT ID: NCT04519333 Completed - Emergencies Clinical Trials

Mesotherapy Versus Systemic Therapy in Treating Neck Pain Related to Herniated Disc

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

Introduction: Neck pain is a global public health concern, that ranked 4th highest health condition in terms of disability as measured by years lived with disability. The aim of this study is to compare the efficiency of one-session mesotherapy application with systemic therapy in treating neck pain related to cervical disk herniation. Methods: This is a prospective parallel randomized controlled trial conducted with patients admitted to our emergency department with neck pain related to cervical disc herniation. A mixture of thiocolchicoside, lidocaine and tenoxicamwas administered via mesotherapy in one group, and intravenous administration of dexketoprofen was applied to the other group. We compared the changes in pain intensity at 60thminute, 120thminute and 24th hours after treatment using Visual Analogue Scale (VAS),and adverse effects of the treatment methods among the study groups.

NCT ID: NCT04519307 Active, not recruiting - Viral Infection Clinical Trials

Evaluation of Newborns Presenting With Suspected COVID 19

Start date: March 1, 2020
Phase:
Study type: Observational

This study evaluates the newborns who had respiratory symptoms at the neonatal intensive care admission

NCT ID: NCT04518527 Completed - Tendinopathy, Elbow Clinical Trials

Efficiency of Kinesio Taping in Chronic Lateral Epicondylitis

Start date: February 1, 2017
Phase: N/A
Study type: Interventional

Lateral epicondylitis is a degenerative tendinosis of the extensor carpi radialis brevis muscle and is the most common work/sports-related chronic musculoskeletal problem affecting the elbow. This randomized, double-blinded, controlled study aimed to evaluate the short term and residual effectiveness of the Kinesio taping method on pain, grip force, quality of life, and functionality.

NCT ID: NCT04518436 Completed - Acute Appendicitis Clinical Trials

Diffusion MRI in Appendicitis

Start date: January 1, 2015
Phase:
Study type: Observational

In this study, it was aimed to investigate the effect of diffusion-weighted magnetic resonance imaging on diagnosis and surgical decision in patients with suspected acute appendicitis. Investigators believe that Diffusion-weighted magnetic resonance imaging is a valuable method in the diagnosis of acute appendicitis and in making the decision of surgery.

NCT ID: NCT04517929 Completed - Clinical trials for Fibromyalgia Syndrome

Effectiveness of Group Psychotherapy in Patients With Fibromyalgia Syndrome

Start date: October 20, 2020
Phase: N/A
Study type: Interventional

The hypothesis of the study is that group therapy in fibromyalgia patients can provide significant improvement in pain, fatigue, anxiety and depression levels and emotional expressions.

NCT ID: NCT04517331 Completed - Pain, Postoperative Clinical Trials

Single and Double Injection Bilateral Thoracic Paravertebral Blocks in Reduction Mammaplasty

Start date: December 1, 2016
Phase: N/A
Study type: Interventional

This study compares the analgesic effects and dermatomal blockade distributions of single and double injection bilateral thoracic paravertebral block (TPVB) techniques in patients undergoing reduction mammaplasty. After obtaining ethics committee approval; 60 patients scheduled for elective bilateral reduction mammoplasty and gave written informed consent, were included in the study. The patients were randomized in one of single (Group S: T3-T4) or double injections (Group D: T2-T3&T4-T5) bilateral TPVB groups (bupivacaine 0.375% 20 mL per side). All patients' dermatomal blockade distributions (T2-T6) were followed for 30 minutes, and then they were given general anesthesia. Before extubation, 1 g IV paracetamol was applied to all. Postoperatively, patients in both groups received IV paracetamol 1 g when numeric rating scale (NRS) pain score ≥4, and also tramadol 1 mg/kg if they defined NRS≥4 again after 1 h. The primary endpoint was NRS pain scores at postoperative 12th hour. The secondary endpoints were NRS scores and dermatomal blockade distributions through the postoperative first 48 hours, postoperative time until first pain, the total numbers of analgesic requirements on days 1 and 2.

NCT ID: NCT04516967 Active, not recruiting - Clinical trials for Immune Thrombocytopenia

Avatrombopag for the Treatment of Thrombocytopenia in Pediatric Subjects With Immune Thrombocytopenia for ≥6 Months

Start date: March 5, 2021
Phase: Phase 3
Study type: Interventional

A Phase 3b Study to Evaluate the Efficacy and Safety of Avatrombopag for the Treatment of Thrombocytopenia in Pediatric Subjects with Immune Thrombocytopenia for ≥6 Months

NCT ID: NCT04516798 Completed - Clinical trials for Reflex, Ankle, Decreased

The Reflex Mechanism Underlying Neuromuscular Effects Of The Whole Body Vibration

WBV-IRM
Start date: October 5, 2020
Phase: N/A
Study type: Interventional

This study was conducted to determine whether the spinal reflex mechanism underlying the neuromuscular effects of whole body vibration (WBV) is tonic vibration reflex. Local and whole body vibration reflex latencies were measured in young adult healthy volunteers.