Clinical trials: Post Discharge
Pulmonary Atelectasis, Morbid Obesity
Use of Airway Pressure Release Ventilation in Morbidly Obese Patients Undergoing Open Heart Surgery
The goal of this Randomized Clinical trial is to to investigate if the use of Air Pressure Release Ventilation in morbidly obese patients undergoing open heart surgery will improve post operative pulmonary outcomes 60 Patients…
- Conditions
- Pulmonary Atelectasis, Morbid Obesity, Pulmonary Complication
- Trial name
- NCT05670483
- Testing
- Use Of APRV mode of Ventilation, Use of conventional Synchronized Intermittent Mandatory Ventilation (SIMV) volume control mode
- Where
- Egypt
- Volunteers
- 60 people
- Sponsor
- Ain Shams University
Pharmacokinetics
A Single Dose, Cross-over Bioequivence Study Comparing Galantamine IR (Immediate Release) Table and Galantmine OS (Oral Solution) in Healthy Volunteers
The purpose of this open-label, single dose, two-treatment, two-period, cross-over study is to evaluate the pharmacokinetic profile and tolerability of galantamine oral solution and galantamine tablet.
- Trial name
- NCT00645554
- Testing
- Galantamine oral solution
- Volunteers
- 2 people, healthy volunteers welcome
- Sponsor
- Xian-Janssen Pharmaceutical Ltd.
Stroke, Disability Physical
Nurse-led Rehabilitation to Improve Self-care Among Stroke Patients in Bangladesh
Stroke causes various levels of disability, which decreases physical function for a prolonged period. The purpose of this study is to test the feasibility and efficacy of a nurse-led rehabilitation program focused on improving…
- Trial name
- NCT06786559
- Testing
- Assistive Device and health Education
- Volunteers
- 64 people
- Sponsor
- Hiroshima University
Melanoma, Complication
Early Complications After Axillary and Inguinal Lymph Node Dissection in Stage III Melanoma Patients
This prospective randomized non-inferiority study is designed to compare the rate and severity of complications after axillary and inguinal lymph node dissection in stage III melanoma patients in a study group where the drain is…
- Trial name
- NCT04680182
- Testing
- Suction drain
- Where
- Norway
- Volunteers
- 104 people
- Sponsor
- Oslo University Hospital
Surgery, Minor
Same Day Discharge for Wedge Resection
Monitoring carefully selected participants to determine if participants can be safely discharged the same day of pulmonary resection
- Conditions
- Surgery, Minor, Lung Cancer
- Trial name
- NCT05067738
- Testing
- same day discharge
- Where
- Canada
- Volunteers
- 54 people
- Sponsor
- London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Healthy Volunteers
Effect of Antacid on Bioavailability of Febuxostat After Administration of a Febuxostat 80 mg Extended-Release Capsule
The purpose of this study is to assess the effect of antacid administration, and its timing, on the bioavailability of a single dose of febuxostat extended-release (XR) 80 mg.
- Trial name
- NCT02382640
- Testing
- Febuxostat XR, Maalox Advance Regular Strength liquid
- Where
- United States
- Volunteers
- 36 people, healthy volunteers welcome
- Sponsor
- Takeda
Hemopatch, Breast Cancer
The Effectiveness of Hemopatch® in the Reduction of Post-surgical Serous Drainage
Hemopatch is an alternative to reduce morbidity associated with axillary lymphadenectomy surgery, possibly contributing to improved patient management, clinical outcomes, and hospital costs.
- Conditions
- Hemopatch, Breast Cancer, Axillary Lymphadenectomy
- Trial name
- NCT04904653
- Testing
- Hemopatch, Control group
- Where
- Spain
- Volunteers
- 118 people
- Sponsor
- Instituto de Investigación Hospital Universitario La Paz
Anterior Knee Pain Syndrome
Lateral Retinacular Release in Total Knee Arthroplasty With Patellar Replacement
The aim of this study is to assess the effect of systematic lateral retinacular release on anterior knee pain, as well as its impact on the functional and radiological outcomes after total knee arthroplasty with patellar…
- Trial name
- NCT05778539
- Testing
- Lateral retinacular release
- Where
- Spain
- Volunteers
- 220 people
- Sponsor
- Hospital del Mar
Stroke
Stroke Rehabilitation, Functional Recovery, and Cost-effectiveness
The investigators will determine the client and non-client variables associated with discharge to an inpatient rehabilitation facility vs. skilled nursing facility in individuals' post-stroke.
- Trial name
- NCT04279977
- Where
- United States
- Volunteers
- 300 people
- Sponsor
- University of Utah
Sepsis
Long-term Assessment of Patients Treated in the ICU for Sepsis
This study is a prospective, observational cohort clinical registry designed to describe clinical and epidemiological characteristics and outcomes of adult patients hospitalized with sepsis.
- Trial name
- LAPTUS (NCT07502794)
- Testing
- Usual Care
- Where
- Brazil
- Volunteers
- 760 people
- Sponsor
- Hospital Israelita Albert Einstein
Rehospitalization
Domiciliary Intervention by Occupational Therapy to Prevent Elderly Rehospitalization
The purpose of this study is to determine whether a home visit by an Occupational Therapist is effective in reducing the rehospitalization rates in elderly patients after hospital discharge.
- Trial name
- NCT02052401
- Testing
- Domiciliary Intervention
- Where
- 2 sites in Chile
- Volunteers
- 206 people
- Sponsor
- Comisión Nacional de Investigación Científica y Tecnológica
Acute Coronary Syndrome
Same-Day Discharge After Coronary Percutaneous Transluminal Coronary Angioplasty (PTCA)
Same day discharge is safe and feasible in selected troponin negative patients undergoing coronary planned percutaneous coronary intervention (PCI) or ad hoc PCI via the transfemoral approach.
- Trial name
- GREECE (NCT01068119)
- Testing
- Same-day discharge
- Where
- United States
- Volunteers
- 57 people
- Sponsor
- Piedmont Healthcare
Pancreatic Disease, Pancreatic Neoplasms
Early (4 Days) Versus Standard Drainage of the Abdominal Cavity After Pancreaticoduodenectomy
Around two thousand pancreaticoduodenectomy (PD) are performed each year in France. This intervention is associated with a high rate of postoperative complications including: pancreatic fistulas (PF); surgical site infections…
- Trial name
- DRAINAGE DPC (NCT01368094)
- Testing
- Drain removal at D4, Standard drain removal
- Where
- 5 sites in France
- Volunteers
- 141 people
- Sponsor
- Centre Hospitalier Universitaire, Amiens
Healthy
Pharmacokinetic Study of Single Doses of ORM-12741
The purpose of this study is to evaluate ORM-12741 concentrations in the blood after different study drug formulations
- Trial name
- Nebula PK 1 (NCT02319057)
- Testing
- ORM-12741 MR A, ORM-12741 IR, ORM-12741 MR B
- Where
- Finland
- Volunteers
- 23 people, healthy volunteers welcome
- Sponsor
- Orion Corporation, Orion Pharma
Acute Pain
How Much Opioids Do You Need After Your Emergency Department Visit
Pain is one of the most common complaints in emergency department (ED) and is still often poorly managed. A major prospective multicenter study reported that 74% of patients that had a pain complaint at ED triage are discharged…
- Trial name
- NCT02799004
- Where
- Canada
- Volunteers
- 761 people
- Sponsor
- Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal
Adult Patients, Intensive Care Unit
Functional Recovery Over the First Year After ICU Discharge
Intensive Care Unit Acquired Delirium (ICU-AD) and Intensive Care Unit Acquired Weakness (ICU-AW) are common in critically ill, mechanically ventilated adult patients.
- Trial name
- NCT04206306
- Where
- Taiwan
- Volunteers
- 407 people
- Sponsor
- National Taiwan University Hospital
Polypharmacy, Deprescription
Reducing Post-discharge Potentially Inappropriate Medications Among Older Adults
Potentially inappropriate medications (PIMs) can lead to adverse drug events (ADEs) among older adults and especially those classified as frail. ADEs are responsible for nearly 27,000 hospital admissions in Canada annually.
- Conditions
- Polypharmacy, Deprescription, Aged
- Trial name
- MedSafer (NCT02918058)
- Testing
- MedSafer
- Where
- Canada
- Volunteers
- 924 people
- Sponsor
- McGill University Health Centre/Research Institute of the McGill University Health Centre
Ost-Mastectomy Shoulder Dysfunction
Effects of Visual-Feedback Induced Therapy and Active Release Technique on Shoulder Pain, Lymphedema, and Functional Disability in Post-Mastectomy Patients.
This randomized controlled trial aims to compare the effects of visual-feedback induced therapy and Active Release Technique on shoulder pain, lymphedema, and functional disability in post-mastectomy patients.
- Trial name
- NCT07719725
- Testing
- Active release technique, Visual-Feedback Induced Therapy
- Where
- Pakistan
- Volunteers
- 44 people
- Sponsor
- Lahore University of Biological and Applied Sciences
Lymphorrhea
Extended-release of Octreotide (LF-PB) for the Treatment of Lymphorrhea
This is a phase II, multicenter, double-blind, double-dummy, parallel-group, placebo-controlled, study to evaluate LF-PB versus placebo in female patients with brest cancer who are undergoing breast surgery with axillary…
- Trial name
- NCT01754285
- Testing
- LF-PB
- Where
- 13 sites in Italy
- Volunteers
- 114 people
- Sponsor
- Chemi S.p.A.
Self Inflicted Injury, Suicide and Self Inflicted Injury
Effects of Community-based Caring Contact on Post-discharge Young Adults With Self-harm
The study will determine whether community-based caring contact via a mobile app connection with or without volunteer support in addition to treatment as usual (psychiatric and psychosocial treatments) has an effect on suicidal…
- Trial name
- NCT03081078
- Testing
- Volunteer support, Mobile app
- Where
- 4 sites in Hong Kong
- Volunteers
- 108 people
- Sponsor
- The University of Hong Kong
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