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Patient Reported Outcomes clinical trials

View clinical trials related to Patient Reported Outcomes.

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NCT ID: NCT04533867 Completed - Pain, Postoperative Clinical Trials

Palonosetron vs. Ondansetron for Postoperative Nausea and Vomiting in Bariatric Surgery

Start date: August 15, 2020
Phase:
Study type: Observational [Patient Registry]

Evaluate the safety and efficacy of palonosetron versus ondansetron to reduce and control post-operative nausea in bariatric surgery.

NCT ID: NCT04236934 Completed - Dyspnea Clinical Trials

Thoracentesis: Symptoms and Prediction of the Need for Therapeutic Thoracentesis

Start date: January 13, 2020
Phase:
Study type: Observational

Recurrent fluid surrounding the lungs is associated with poor quality of life, the main symptom being dyspnea. These patients are in need of recurrent removal of the fluid using drainage. The mechanism causing dyspnea is not fully understood. By using ultrasound to evaluate the movement of the diaphragm before and after removal of fluid and the patients symptoms before removal of fluid and until next removal the research group aims to clarify the temporal development in symptoms and the role of the diaphragm. The researchers will also evaluate the ability of the pulmonologist and patient to predict when the patient will need the next removal of fluid in patients with recurrent unilateral pleural effusion.

NCT ID: NCT03435484 Completed - Clinical trials for Patient-reported Outcomes

Using RCT to Increase Completion Rates of the Health Assessment Questionnaire.

Start date: February 7, 2018
Phase: N/A
Study type: Interventional

The proposed study aims to examine several iterations of instructions/reminders that patients receive for completing the Health Assessment Questionnaire (self-reported health outcomes) for their outpatient visit at NYU Langone Orthopedic Center. The goal is to increase the completion rates of patient-reported health outcomes.

NCT ID: NCT03341377 Completed - Clinical trials for Patient-reported Outcomes

Perioperative Symptom Study of Lung Cancer (CN-PRO-Lung 1)

Start date: November 21, 2017
Phase:
Study type: Observational

Investigators propose a multicenter prospective observational cohort study to develop and validate essential technical parameters for establishing the patient-reported outcome-based perioperative symptom management cohort in patients with lung cancer. With at least 300 patients with initial diagnosis of lung cancer and scheduled for surgery, this study will administer symptom assessments (MDASI-LC) and quality of life assessments (SIQOL) before surgery (typically within 3 days before surgery), daily after surgery (in hospital ≤ 14 days), and weekly after discharge, up to 4 weeks (±3 days) or the start day of postoperative oncologic treatment. In the upgraded research protocol, symptom and quality of life assessments (every 3 month for 1 year, every 6 month for 2-3 year, every 12 month for 4-5 year), as well as the follow-up of clinical outcomes will continue until 5 years after surgery.

NCT ID: NCT03228342 Completed - Clinical trials for Rheumatoid Arthritis

Ultrasound Impact in Rheumatoid Arthritis Patient Reported Outcomes

ULTRAPRO
Start date: May 3, 2017
Phase: N/A
Study type: Interventional

Evaluate the impact of MusculoSkeletal Ultrasound added to Rheumatoid Arthritis patients classified in remission/low disease activity in terms of Patient Reported Outcomes.

NCT ID: NCT03178045 Completed - Clinical trials for Patient Reported Outcomes

Ambulatory Cancer Care Electronic Symptom Self-Reporting for Surgical Patients

Start date: May 31, 2017
Phase:
Study type: Observational

The aim of this study is to understand and improve the experience of patients after surgery by comparing two methods of following symptoms while the patient recovers at home.