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NCT ID: NCT04594434 Completed - Clinical trials for Complex Post-Traumatic Stress Disorder

Eye Movement Desensitization and Reprocessing (EMDR) in Complex Psychotrauma

Start date: December 12, 2020
Phase: N/A
Study type: Interventional

This study wants to demonstrate the effectiveness of combining a positive memory with "recommended" therapy based on EMDR in reducing the disturbance that patients with complex psychotrauma may experience. The positive memory will be called "benevolent memory" (SB) or "less worse memory" (SMP).

NCT ID: NCT04594213 Completed - Clinical trials for Moderate to Severe Upper Facial Lines (Horizontal Forehead Lines, Glabellar Frown Lines, and Lateral Canthal Lines)

Safety and Efficacy Study of the Simultaneous Treatment of Upper Facial Lines (Horizontal Forehead Lines, Glabellar Frown Lines and Lateral Canthal Lines) in Subjects With Moderate to Severe Upper Facial Lines

ULTRA I
Start date: September 23, 2020
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the safety and efficacy of NT 201 (active ingredient: Botulinum (neuro)toxin type A, free from complexing proteins) in the combined treatment of wrinkles in the upper face (Upper Facial Lines [UFL]): Horizontal Forehead Lines [HFL], Glabellar Frown Lines [GFL], and Lateral Canthal Lines [LCL]). It is a prospective, randomized, double-blind, placebo-controlled, multicenter study with a placebo-control main period (MP) followed by an open-label extension (OLEX) period.

NCT ID: NCT04594161 Completed - Kidney Diseases Clinical Trials

Effectiveness of Drainage by PCN vs. JJ in Patients With Symptoms of Obstructive Kidney Disease Caused by Urolithiasis

STONE
Start date: July 15, 2020
Phase: N/A
Study type: Interventional

To investigate the effectiveness of percutaneous nephrostomy catheter placement versus retrograde double J catheter placement in patients with symptoms of obstructive kidney disease (with either infection and/or pain and/or kidney function deterioration) caused by urolithiasis.

NCT ID: NCT04593927 Completed - Clinical trials for Secondary Progressive Multiple Sclerosis (SPMS)

Long Term Special Drug Use-results Surveillance for Mayzent in SPMS Patients

Start date: October 28, 2020
Phase:
Study type: Observational

This study is a single cohort, central registration system, all-case, open-label, multicenter observational study in patients using Mayzent for the indication of secondary progressive multiple sclerosis.

NCT ID: NCT04593576 Completed - Clinical trials for Autistic Disorder of Childhood Onset With Full Syndrome

Impact of Sports Activity on Pragmatic Skills of Children

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

To investigate the effects of structured physical exercises/outdoor sports on social interaction/communication skills of children with Autism in Pakistan.

NCT ID: NCT04593550 Completed - Clinical trials for Malignant Female Reproductive System Neoplasm

Electroencephalographic Changes Under General Anesthesia in Patients With Gynecologic Cancers With and Without History of Chemotherapy

Start date: July 31, 2020
Phase:
Study type: Observational

This study compares changes in brain waves in women with gynecologic cancers who have or have not received chemotherapy and who are scheduled to receive surgery as part of their standard care. Electroencephalography is a test that measures brain waves and may help learn if sensitivity to anesthesia is higher in women who have received chemotherapy than women who have not. This study may help researchers learn if receiving chemotherapy before surgery can affect the way the brain responds to anesthesia during and after surgery.

NCT ID: NCT04593264 Completed - Clinical trials for Anterior Cruciate Ligament Injuries

Quantifying the Benefits of Supervised vs. Unsupervised Pre-habilitation for Patients With Acute ACL Tears

Start date: February 23, 2021
Phase: N/A
Study type: Interventional

Although the success of physical therapy following surgery has been well-documented and validated in patients undergoing Anterior Cruciate Ligament Reconstruction (ACLR) procedures, more recent studies have demonstrated that patient outcomes are the most favorable when surgery is delayed approximately 4 weeks until after the patient has completed a preoperative physical therapy program, or "pre-habilitation." The ultimate goal of pre-habilitation is to regain full range of motion in the knee and reach approximately 80% of pre-injury quadricep strength. However, extra physical therapy can stress both time and resources. Thus, we propose a home-based, self-guided pre-habilitation program. We hypothesize that patients participating in self-guided pre-habilitation will experience the same benefits as patients in a traditional office-based physical therapy program.

NCT ID: NCT04592783 Completed - Clinical trials for Hypertension in the Obstetric Context

Postpartum Hypertension, Tight vs Liberal Control Trial

Start date: October 19, 2020
Phase: N/A
Study type: Interventional

To determine if treatment of less severe hypertension in the postpartum period results in a lower frequency of maternal morbidity.

NCT ID: NCT04592718 Completed - Anxiety Clinical Trials

Four-week Breathing Interventions on Gut Symptoms, Heart Rate Variability, and Psychological Measures in Runners

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

Recent research has suggested that stress and anxiety levels are associated with gastrointestinal (GI) symptoms in endurance athletes (runners, cyclists, triathletes). Yet, there has been limited attempt to evaluate whether GI symptoms during running can be mitigated by interventions designed to reduce stress and anxiety. Thus, this study will evaluate the effects of four-week slow deep breathing and mindful breath counting interventions on subjective and objective measures of stress/anxiety and GI symptoms in runners with mild-to-high anxiety and that are prone to GI symptoms during runs.

NCT ID: NCT04592406 Completed - Clinical trials for Contrast-induced Nephropathy

Data on the Prevention of Complications of Prophylactic Intravenous Hydration in Patients With eGFR < 30

CVP
Start date: December 1, 2018
Phase:
Study type: Observational

At Maastricht University Medical Centre (Maastricht UMC+) a specialised unit was established where a dual screening process including both renal and cardiac parameters is used to minimize the risk of contrast-induced acute kidney injury as well as the risk of prophylactic hydration in eGFR<30mL/min/1.73m2 patients. Very little data exists on patients with eGFR <30mL/min/1.73m2 in this context. The current study aims to describe post-contrast outcomes of patients to whom this screening method has been applied.