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Iatrogenic Injury clinical trials

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NCT ID: NCT06078527 Not yet recruiting - Aspiration Clinical Trials

Assessment of Laryngopharyngeal Sensation: Cancer Survivor Cohort

Start date: August 1, 2024
Phase: N/A
Study type: Interventional

A previous study completed in 2022 (NCT05158179) was conducted using cohorts of healthy controls, and adults with general laryngopharyngeal disorders. This study will expand on the previous research to include a separate cohort of adults being seen in clinic for an existing laryngopharyngeal disorder resulting from previous radiation or other cancer treatments.

NCT ID: NCT05712850 Enrolling by invitation - Clinical trials for Sacroiliac Joint Dysfunction

Clinical Outcome and Fusion Results Using the SiJoin® Transfixing Sacroiliac Fusion Device

Start date: January 19, 2023
Phase:
Study type: Observational

The purpose of this clinical study is to evaluate fusion of the SI joint(s) and any reduction in VAS pain scores in a prospective cohort of patients utilizing the SiJoin® Transfixing Sacroiliac Fusion Device in patients that received sacroiliac fusion, without ancillary stabilization devices.

NCT ID: NCT04990700 Completed - Pain, Postoperative Clinical Trials

Effect of Partial Rib Resection On the Control of Post-thoracotomy Pain

Start date: May 9, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the effect of partial rib resection in reducing acute post-thoracotomy pain

NCT ID: NCT01536340 Completed - Iatrogenic Injury Clinical Trials

Identifying Adverse Events After Discharge From a Community Hospital

Start date: September 2011
Phase: N/A
Study type: Observational

The purpose of this study is to: -Determine the incidence of adverse events, preventable adverse events, and ameliorable adverse events, and the timeliness of post-discharge ambulatory appointments, affecting urban and rural patients approximately 3-4 weeks after discharge from a hospitalist-run medical service of a large community hospital to home. H1: The incidence of post-discharge adverse events will be higher in rural patients compared with urban patients discharged from a hospitalist-run medical service of a large community hospital. -Identify and classify the types of post-discharge adverse events (e.g., adverse drug events, procedure-related events, hospital acquired (nosocomial) infections, falls, and other) affecting urban and rural patients approximately 3-4 weeks after discharge from a hospitalist-run medical service of a large community hospital to home. H2: All patients will be at higher risk for adverse drug events than other types of adverse events. -Examine the relationships between the population at risk, characteristics of the health care delivery system, and the utilization of post-discharge health services, and how these relationships help us understand the incidence of post-discharge adverse events. H3: Several factors will be independently associated with the incidence of post-discharge adverse events in rural and urban patients, including patient comorbidity, severity of acute illness, presence of a primary care physician prior to hospitalization, and a scheduled timely post-discharge ambulatory follow-up appointment.