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NCT ID: NCT04187352 Completed - Clinical trials for Unresectable Locally Advanced, Recurrent or Metastatic Esophageal Squamous Cell Carcinoma

A Study of CS1001 in Subjects With Esophageal Squamous Cell Carcinoma

Start date: December 19, 2019
Phase: Phase 3
Study type: Interventional

Phase III Study to Investigate the Efficacy and Safety of CS1001 or Placebo in Combination with FP as First-Line Therapy in Subjects with Unresectable Locally Advanced, Recurrent or Metastatic Esophageal Squamous Cell Carcinoma

NCT ID: NCT04186923 Completed - Clinical trials for Families With Minor Children and One Parent Suffering From Cancer

Familien-SCOUT: Comprehensive Support for Families With a Parent Suffering From Cancer

F-SCOUT
Start date: October 1, 2019
Phase: N/A
Study type: Interventional

When a parent with minor children falls ill with cancer, it is extremely stressful for all of the family members, including the partner and children. Familiar everyday routines are often disrupted even at an early stage, and for a prolonged period. Financial difficulties, the threat represented by the uncertain course of the disease, and worries about the children's future have a cumulative effect. The affected families are thereby pushed to their limits organizationally and emotionally. The burden involved tends to be underestimated, and secondary psychological conditions often develop among all the family members. They often do not have adequate access to support. The aim of this project is to establish a care management system that provides support for families with underage children in which one parent is seriously ill. In order to reduce the burden on families, "family SCOUTS" are to be used who can provide advice and information at an early stage. They are intended to encourage families to discuss things openly, and they should also facilitate access to all the support services available. The project will evaluate whether the use of family SCOUTS reduces the burden on the family in comparison with families who do not have a family SCOUT. For this purpose, investigations will be carried out before and after the family SCOUTS are deployed. Standardized questionnaires, interviews, and routine data from the participating health-insurance companies will provide the basic data.

NCT ID: NCT04186897 Completed - Clinical trials for Symptomatic Irreversible Pulpitis

Occlusal Reduction Effect on Postendodontic Pain

Start date: September 2014
Phase: N/A
Study type: Interventional

The aim of this study, thus, was to assess the effect of occlusal reduction on postendodontic pain after the first (post-instrumentation) and the second (post-obturation) visit in mandibular posterior teeth with symptomatic irreversible pulpitis and sensitivity to percussion treated in two visits.

NCT ID: NCT04186884 Completed - Clinical trials for Advanced Malignant Neoplasm

Caregiver Burden, Quality of Life, and Symptom Distress at Different Palliative Cancer Care Settings

Start date: March 26, 2019
Phase:
Study type: Observational

This trial studies caregiver burden, quality of life, and symptom distress of patients and their informal (unpaid) caregivers at different palliative care settings. Cancer caregiving may affect a caregiver's life physically, emotionally, socially, and financially. Studying caregiver burden may help investigators learn about caregivers' opinions on stress of caregiving, and about the factors related to caregiver burdens.

NCT ID: NCT04186702 Completed - Clinical trials for Diabetes Mellitus, With Complications

New Concepts in Diabetic Macular Edema (DME)

DME
Start date: September 10, 2014
Phase: N/A
Study type: Interventional

Intravitreal ranibizumab injection procedure is simple and effective. In management of chronic DME there is no clear anatomical endpoint. Visual stability is the primary aim. Argon focal laser therapy can be the safe second choice. The combined therapy is successful and practical for chronic DME patients.

NCT ID: NCT04186676 Completed - Clinical trials for Acute Myocardial Infarction

Myocardial Infarction With Non-Obstructive Coronary Arteries in the Greek Population

MINOCA-GR
Start date: January 1, 2021
Phase:
Study type: Observational [Patient Registry]

The MINOCA-GR registry will be the first nationwide study aiming to obtain data regarding prevalence, demographics, clinical profile, previous anginal status, presence of cardiovascular risk factors, management and outcomes in patients with Myocardial Infarction with Non-Obstructive Coronary Arteries. An additional purpose of the registry is to highlight, for the first time worldwide to the best of the investigator's knowledge, the role of cardiac computed tomography angiography for risk stratification and personalized therapeutic approach in MINOCA patients.

NCT ID: NCT04186598 Completed - Clinical trials for Continuous Positive Airway Pressure

Evaluating the Utility of Continuous Positive Airway Pressure in the Treatment of High Altitude Pulmonary Edema

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

The primary objective is to evaluate the efficacy of continuous positive pressure on resolution of high-altitude pulmonary edema vs high flow oxygen. The secondary objective is to derive an incidence of high-altitude pulmonary edema based on the elevation and timing from which the subject arrives. Additionally, in a convenience sample of the base study population, an ultrasound evaluation for the presence of B lines in the lungs will be conducted after 2 hours.

NCT ID: NCT04186481 Completed - Clinical trials for Achilles Tendon Repairs/Reconstructions

A Study of the Safety and Performance of the MINITACâ—Š Titanium 2.0 Suture Anchor

MINITAC
Start date: October 25, 2019
Phase:
Study type: Observational

This is a retrospective study evaluating the safety and performance of the MINITAC Suture anchors for extremities repair. Data will be used to support Notified Body (BSI) requirements for extremities repair indications.

NCT ID: NCT04186312 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder

A Psychosocial Treatment Program for College Students (ACCESS)

ACCESS
Start date: August 1, 2015
Phase: N/A
Study type: Interventional

The results of this study are expected to provide important and new information regarding the treatment of academic impairment among college students with ADHD. The present study should provide a substantial addition to the existing knowledge base concerning interventions for college students with ADHD. In addition, because the intervention is being implemented during college, potential benefits include the prevention of the severe academic and psychosocial functioning difficulties associated with ADHD, including school dropout.

NCT ID: NCT04186091 Completed - Clinical trials for Perfusion Index Predicts Post-spinal Hypotension

Perfusion Index Predicts Post-spinal Hypotension in Obese Parturients for Cesarean Section

Start date: April 1, 2017
Phase:
Study type: Observational [Patient Registry]

Hypotension is a common adverse effect of spinal anesthesia during caesarean section especially in obese patients. The aim of this study is to find out the correlation between baseline PI and post spinal hypotension in obese parturient.