Clinical trials: Post Discharge
Diabetes
Use of CGM for Diabetes Management Following a Hospitalization.
Patients with diabetes hospitalized for heart failure or acute myocardial infarction will have a continuous glucose monitor (CGM) placed on the day of discharge which will be downloaded at their outpatient follow up clinic visit…
- Trial name
- NCT04149392
- Testing
- Continuous Glucose Monitor
- Sponsor
- University of Virginia
Patient Discharge, Urinary Complication
Postoperative Bladder Filling After Outpatient Laparoscopic Hysterectomy and Time to Discharge
The investigators hypothesize that backfilling the bladder postoperatively will reduce time to spontaneous void and subsequent discharge from the post-anesthesia care unit.
- Trial name
- NCT06737393
- Testing
- Backfill
- Where
- United States
- Volunteers
- 112 people, healthy volunteers welcome
- Sponsor
- University of Tennessee
Healthy
Bioavailability of Dipyridamole of Asasantin p.o. in Three Experimental Formulations Relative to the Standard Formulation in Healthy Male Subjects
The objective of this study was to compare the pharmacokinetics of dipyridamole in three different Asasantin ER batches (test) containing different amounts of retarding lacquers to the existing commercial product at steady state…
- Trial name
- NCT02273557
- Testing
- Asasantin ER (new formulation I - low), Asasantin ER (new formulation III - medium), Asasantin ER (new formulation II - high)
- Volunteers
- 19 people, healthy volunteers welcome
- Sponsor
- Boehringer Ingelheim
ADHD
Amphetamine Extended Release Tablets and Driving Performance in Subjects With Attention Deficit/Hyperactivity Disorder (ADHD)
The purpose of this study is to assess the effect on driving performance of a single dose of amphetamine extended-release tablets (20 mg/tablet) compared with placebo at 45 minutes and 10 hours post-dose in young adults with ADHD.
- Trial name
- NCT04027361
- Testing
- Amphetamine Extended Release (ER) Tablet 20 mg
- Where
- United States
- Volunteers
- 41 people
- Sponsor
- Tris Pharma, Inc.
Critical Illness, Intensive Care
Exercise After Intensive Care Unit: a Randomised Controlled Trial
The purpose of this study is to test if a 6-week programme of exercise improves physical function and health related quality of life in patients following intensive care who are discharged from hospital.
- Trial name
- REVIVE (NCT01463579)
- Testing
- Exercise Programme, Standard Care
- Where
- 5 sites in United Kingdom
- Volunteers
- 60 people
- Sponsor
- University of Ulster
Heart Failure, Congestive, Coronary Arteriosclerosis
After Discharge Management of Low Income Frail Elderly
The purpose of this study is to determine whether comprehensive post-hospitalization interdisciplinary care management can be an effective care delivery model to improve outcomes in low-income frail elderly.
- Conditions
- Heart Failure, Congestive, Coronary Arteriosclerosis, Atrial Fibrillation, Cerebrovascular Accident
- Trial name
- NCT00328848
- Testing
- Behavioral
- Volunteers
- 530 people
- Sponsor
- Summa Health System
Post-Acute-Stroke Rehabilitation
Effectiveness of a Wearable Device-based Assisted Post-stroke Rehabilitation System
Multidisciplinary rehabilitation facilitates functional recovery after stroke, and adherence to rehabilitation guidelines is associated with improved outcomes.
- Trial name
- NCT04997408
- Testing
- Customized exercise app, In-person therapist-supervised rehabilitation
- Volunteers
- 140 people
- Sponsor
- Landseed Hospital
Posttransplant Diabetes Mellitus
Tacrolimus Formulation and Glucose Metabolism After Kidney Transplantation (TAGLUMET Trial)
Posttransplantation diabetes mellitus after kidney transplantation mediated by tacrolimus is mainly dependent on dose and peak plasma concentration.
- Trial name
- TAGLUMET (NCT05396898)
- Testing
- LCP-tacrolimus, twice-daily tacrolimus
- Where
- Germany
- Volunteers
- 44 people
- Sponsor
- University Hospital Tuebingen
Covid19, SARS-CoV2
Resistance Training and Clinical Status in Patients With Post Discharge Symptoms After Covid-19
COVID-19 survivors commonly exhibit a marked extra-respiratory complication affecting the cardiac (arrhythmias and myocardial injury), renal (acute kidney injury), gastrointestinal, nervous (neuropathy, encephalopathy), endocrine…
- Conditions
- Covid19, SARS-CoV2, Fatigue Syndrome, Chronic, Stress, Psychological
- Trial name
- EXER-COVID (NCT04797871)
- Testing
- Resistance training, Standard care
- Where
- Spain
- Volunteers
- 100 people
- Sponsor
- Universidad Pública de Navarra
Concussion
Concussion Texting Study
This will be a prospective study of the implementation of a real-time assessment and intervention of a text messaging tool in mild traumatic brain injury (mTBI) patients post-discharge from the emergency department.
- Trial name
- texting (NCT03099733)
- Testing
- text message
- Where
- United States
- Volunteers
- 40 people
- Sponsor
- Wake Forest University Health Sciences
Cervicogenic Headache
Effects of Sub-Occipital Myofascial Release in Patients With Cervicogenic Headache
Cervicogenic headache is a secondary form of headache that occurs from the upper cervical spine and atlanto-occipital joint. A CGH is a frequent source of chronic headache and is frequently misdiagnosed .Cervicogenic headache is…
- Trial name
- NCT04816448
- Testing
- cervical mobilization (Headache SNAG), Sub-occipital myofascial release
- Where
- Pakistan
- Volunteers
- 22 people
- Sponsor
- Riphah International University
Cellulite
Extracorporeal Shock Wave Therapy Versus Manual Lymphatic Drainageon Cellulite Post Liposuction
To determine whether extracorporeal shock wave therapy (ESWT) or manual lymphatic drainage (MLD) is more effective for decreasing post-liposuction cellulite.
- Trial name
- NCT04498312
- Testing
- Extracorporeal shock wave
- Where
- Egypt
- Volunteers
- 30 people
- Sponsor
- Cairo University
Trauma
Registry AutoLog Lipid Removal and Blood Component Characterization
The purpose of this study is to show the success of the AutoLog System in removing lipids to less than 10mg/dl in vivo. The Autolog registry has two objectives: 1.
- Trial name
- NCT01565967
- Where
- 6 sites in Italy, Lithuania and 4 more
- Volunteers
- 199 people
- Sponsor
- Medtronic Cardiac Rhythm and Heart Failure
Trigger Finger, Hyaluronic Acid
Evaluate the Effectiveness of Crosslinked HA on the Adhesion Preventing After Trigger Finger Release Surgery
To Evaluate the Effectiveness of the use of a Novel Crosslinking Hyaluronan Hydrogel on the Prevention of the Adhesion Occurrence After Trigger Finger Release Surgery
- Trial name
- NCT05082480
- Testing
- Hyaluronic acid (HA), Saline
- Where
- 2 sites in Taiwan
- Volunteers
- 5 people
- Sponsor
- SciVision Biotech Inc.
Frailty, Dependence
Bridging the Gap: Creating a Continuum of Care
Coordination and integration between care settings is essential for the quality of care of frail older patients. An active follow-up by a case manager (CM) after discharge form an acute geriatric hospital ward has the potential…
- Conditions
- Frailty, Dependence, Integrated Care
- Trial name
- NCT06368674
- Testing
- Intervention group Case Manager (CM), Control Group
- Where
- Sweden
- Volunteers
- 150 people
- Sponsor
- Göteborg University
Opioid Use Disorder
Reentry Incentives and Support for Engagement With Contingency Management
People leaving jail face a very high risk of overdose, especially in the first few weeks after release. Staying on medication for opioid use disorder (MOUD) can greatly reduce this risk, but many people stop treatment during this…
- Trial name
- RISE-CM (NCT07322588)
- Testing
- Reentry Incentives and Support for Engagement with Contingency Management (RISE-CM) Intervention
- Where
- United States
- Volunteers
- 75 people
- Sponsor
- Oregon Health and Science University
Post-ERCP Pancreatitis, Pancreatitis
Short-Stay Aggressive Hydration to Prevent Post-ERCP Pancreatitis
Post-ERCP pancreatitis (PEP) is the most common serious adverse event after endoscopic retrograde cholangiopancreatography (ERCP), occurring in roughly 7-15% of patients.
- Trial name
- PuSH (NCT07776561)
- Testing
- Short-Stay Aggressive Hydration, Standard Peri-procedural Hydration, Rectal Indomethacin
- Where
- Australia
- Volunteers
- 1,300 people
- Sponsor
- Westmead Hospital
Breast Cancer Females
"Topical Tranexamic Acid With Flap Fixation: A Novel Approach to Minimize Post-operative Drainage and Surgical Site Infection in Patients Undergoing Modified Radical Mastectomy"
Seroma (a collection of fluid under the skin) is a common problem after breast cancer surgery, especially after modified radical mastectomy (MRM), where lymph nodes from the armpit are also removed.
- Trial name
- NCT07434453
- Testing
- Tranexamic Acid (Topical Application in Mastectomy Wound), flap fixation
- Where
- Pakistan
- Volunteers
- 62 people
- Sponsor
- Noor ul Ain
Breast Cancer, Mastectomy; Lymphedema
Same-Day Discharge After Nipple-sparing Mastectomy or Skin-sparing Mastectomy With Breast Reconstruction
This novel study will assess the feasibility and outcomes of same-day discharge following mastectomy with implant-based pre-pectoral reconstruction.
- Conditions
- Breast Cancer, Mastectomy; Lymphedema, Same Day Surgery, Nipple-sparing Mastectomy
- Trial name
- NCT04596683
- Testing
- Same-day NSM or SSM
- Where
- 3 sites in United States
- Volunteers
- 60 people
- Sponsor
- Georgetown University
Heat Effect
Effect of Heat on Oxybutynin Release and Absorption From Oxybutynin Products
This research study is intended to determine the effect of heat and occlusion on oxybutynin products.
- Trial name
- NCT03205605
- Testing
- oxybutynin
- Where
- United States
- Volunteers
- 13 people, healthy volunteers welcome
- Sponsor
- University of Maryland, Baltimore
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