Clinical trials: Post Discharge
Hospital Mortality
International Multicenter Study of In-hospital Outcome of Patients After ICU Discharge
Several patients die in the intensive care unit (ICU) due to their acute disease and comorbid conditions. Moreover, after ICU discharge, some ICU survivors still die in the wards.
- Trial name
- NCT02347150
- Where
- 3 sites in Portugal
- Volunteers
- 3,000 people
- Sponsor
- Hospital Vila Franca de Xira
Mental Illness
Recovery Bridge: Peer Intervention to Bridge Transition Post Discharge
The time following discharge from psychiatric hospitalization is a high-risk period and has been associated with a range of negative outcomes including high rates of hospital readmission and suicide.
- Trial name
- NCT05758376
- Testing
- Recovery Bridge
- Where
- United States
- Volunteers
- 15 people, healthy volunteers welcome
- Sponsor
- VA Office of Research and Development
Acute Kidney Injury
Maximizing Acute Kidney Injury End-point Intervention Post-Discharge (MAKE-IT) Study
This purpose of this pilot and feasibility study is to determine whether attending an acute kidney injury (AKI) clinic after discharge from the hospital impacts prescription medicine use, blood pressure and recovery of kidney…
- Trial name
- MAKE-IT (NCT04358874)
- Testing
- Medication reconciliation, Blood Pressure Management
- Where
- 3 sites in United States
- Volunteers
- 20 people
- Sponsor
- University of Alabama at Birmingham
Symptoms and Signs, Symptom Cluster
Patient Reported Symptoms the First Week After Intensive Care Unit Discharge and up to Hospital Discharge
The overall objective of this study is a) to increase knowledge about ICU patient's symptoms and symptom clusters during the first week after ICU discharge, and b) to identify cognitive, psychological, and physical symptoms and…
- Conditions
- Symptoms and Signs, Symptom Cluster, Follow-up Care, Critical Illness
- Trial name
- NCT05266118
- Where
- 2 sites in Norway
- Volunteers
- 177 people
- Sponsor
- Ostfold Hospital Trust
Nursing, Gynecological Cancers
Effects of a Self-Regulation Based E-MOTE Program Delivered Via an AI-Assisted Robot and Supported by Mobile Platforms for Newly Diagnosed Gynecologic Cancer Patients
To evaluate the effectiveness of the E-MOTE Emotional Care Program, delivered through the Kebbi robot and the LINE Official Account, for patients newly diagnosed with gynecologic cancer undergoing surgery.
- Conditions
- Nursing, Gynecological Cancers, Psycho-Oncology
- Trial name
- NCT07745478
- Testing
- E-MOTE group
- Where
- Taiwan
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- National Taiwan University Hospital
Vital Sign, Clinical Deterioration
WARD-Home - Continuous Monitoring of Vital Parameters After Discharge
The current pilot study aims to investigate the feasibility of wireless, continuous monitoring of patients in the days around discharge after an acute medical hospitalization, as well as occurrence of deviating vital signs in…
- Trial name
- NCT05223504
- Testing
- Continuously monitoring
- Where
- Denmark
- Volunteers
- 80 people
- Sponsor
- Copenhagen University Hospital, Rigshospitalet
Surgery, Opioid Use
Opioid Prescribing After Cesarean Delivery
The number of opioid overdose deaths in the United States has quadrupled in 15 years, a dramatic manifestation of the current opioid abuse epidemic.
- Trial name
- NCT03168425
- Testing
- Tailored prescription, Control
- Where
- United States
- Volunteers
- 190 people, healthy volunteers welcome
- Sponsor
- Vanderbilt University Medical Center
Diabetes, Dyslipidemia
Strategies to Maintain Cardiac Risk Control After Discharge From Cardiovascular Risk Reduction Clinic
The purpose of this study is to determine whether a combined behavioral and pharmacological intervention provided by a multidisciplinary team will further reduce LDL-C, smoking, BP and Hb-A1C in diabetic patients with A1c between…
- Conditions
- Diabetes, Dyslipidemia, Hypertension, Coronary Atherosclerosis
- Trial name
- NCT00358033
- Testing
- Counseling, Interactive Education, Group Support
- Where
- United States
- Volunteers
- 200 people
- Sponsor
- Providence VA Medical Center
Hand Burn, Carpal Tunnel Syndrome
Shock Wave on Pillar Pain After Carpal Tunnel Release in Hand Burn
"In burn cases, the reported causes of CTS are increased volume of carpal tunnel content due to edema and synovitis, wrist hyperextension, tight dressing, fibrosis, and direct burn to the nerve.
- Trial name
- NCT06371885
- Testing
- shock wave therapy, traditional physical therapy
- Where
- Egypt
- Volunteers
- 52 people
- Sponsor
- Cairo University
Pancreatic Carcinoma
Accelerated Recovery Pathway for Discharge After Surgery in Patients With Pancreatic Cancer
This randomized clinical trial studies accelerated recovery pathway for discharge after surgery in patients with pancreatic cancer.
- Trial name
- WARP (NCT02517268)
- Testing
- Pancreaticoduodenectomy
- Where
- United States
- Volunteers
- 98 people
- Sponsor
- Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University
Transthyretin Amyloidosis, Transthyretin Cardiac Amyloidosis
Prevalence of wtATTR-CM After Carpal Tunnel Release Surgery
Patients above the age of 60 will be recruited at their carpal tunnel release surgery. Biopsies will be taken from the wrist and examined for the presence of amyloid protein.
- Conditions
- Transthyretin Amyloidosis, Transthyretin Cardiac Amyloidosis, Wild-Type Transthyretin-Related (ATTR)Amyloidosis
- Trial name
- CACTuS2 (NCT04276220)
- Testing
- Tenosynovial biopsy
- Where
- Denmark
- Volunteers
- 109 people
- Sponsor
- Steen Hvitfeldt Poulsen
Cigarette Smoking, Tobacco Smoking
Comparative Effectiveness of Post-Discharge Strategies for Hospitalized Smokers
Cigarette smoking is the leading preventable cause of death in the U.S. The 2008 US Public Health Service Smoking Cessation Guideline recommends offering effective treatment to smokers in all health care settings, including…
- Conditions
- Cigarette Smoking, Tobacco Smoking, Tobacco Use Disorder
- Trial name
- Helping HAND2 (NCT01714323)
- Testing
- Sustained Care, Standard Care
- Where
- 3 sites in United States
- Volunteers
- 1,359 people
- Sponsor
- Massachusetts General Hospital
Postoperative Nausea and Vomiting
Impact of Drains on Postoperative Nausea and Vomiting After Thyroid Surgery
Wound Drains after Thyroid- and Parathyroid Surgery Impact on Postoperative Nausea and Vomiting (PONV)
- Trial name
- PONTS (NCT01679418)
- Testing
- Placement of a wound drain post surgery (Redon; Medicoplast), No-drain after surgery
- Where
- Switzerland
- Volunteers
- 139 people
- Sponsor
- Kantonsspital Liestal
Hypertension
Efficacy and Safety of Metoprolol Succinate Prolonged-Release Tablet in Patients With Mild to Moderate Hypertension
This is an open-label, non-comparative, multi-centre clinical study to evaluate the Efficacy and safety of Metoprolol Succinate prolonged-release tablet (Betaloc Zok) in patients with mild to moderate essential hypertension.
- Trial name
- NCT00861016
- Testing
- metoprolol succinate prolonged-release tablet and felodipine
- Volunteers
- 310 people
- Sponsor
- AstraZeneca
Knee Arthroscopy, Meniscus
Temperature Sensitive Release of PGE2 and Diminished Energy Requirements in Synovial Tissue With Postoperative Cryotherapy - A Prospective Randomised Study After Knee Arthroscopy
Abstract Background: Local external cooling of the postoperative field is a treatment paradigm aiming for enhanced recovery after joint surgery. It is supposed to reduce pain and improve mobilization, enabling same day surgery.
- Conditions
- Knee Arthroscopy, Meniscus, Inflammation, Hydrops
- Trial name
- NCT01247376
- Testing
- Cooling and compression
- Where
- Sweden
- Volunteers
- 40 people
- Sponsor
- Karolinska Institutet
Critically Ill Patients
Effects of Compound Ejiao Syrup on Exercise Tolerance and Quality of Life in Critically Ill Patients After ICU Discharge: A Double-Blind, Multicenter,Randomized Controlled Clinical Study
This study, titled "Effect of Compound Ejiao Jiang on Exercise Tolerance and Quality of Life of Critically Ill Patients after Discharge from ICU: A Double-Blind, Multicenter, Randomized Controlled Clinical Study (LIFT Study),"…
- Trial name
- NCT07157748
- Testing
- Fufang E'jiao Jiang
- Where
- China
- Volunteers
- 178 people
- Sponsor
- Third Military Medical University
Schizophrenia, Schizoaffective Disorder
As Study of the Pharmacokinetics of Paliperidone Extended-release and Risperidone Immediate-release Formulations
The purpose of this study is to compare the steady-state pharmacokinetics of paliperidone after oral administration of 15 mg extended-release (ER) OROS paliperidone once daily with the steady-state pharmacokinetics of…
- Trial name
- NCT00796185
- Testing
- Paliperidone ER
- Volunteers
- 62 people
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Dupuytren's Disease
Splinting for Dupuytren's Contracture Release
This study is comparing two different kinds of splints for patients who have had a surgical contracture release of dupuytren's disease. It compares a static splint and a dynamic splint.
- Trial name
- NCT00575458
- Where
- United States
- Volunteers
- 60 people
- Sponsor
- Massachusetts General Hospital
Arthrogenic Muscle Inhibition, Knee Injuries
Effect of Surface EMG Biofeedback on Quadriceps Inhibition Release During Postoperative Knee Rehabilitation
Arthrogenic muscle inhibition (AMI) is a common neurological impairment following knee surgery that limits voluntary quadriceps activation and delays functional recovery.
- Conditions
- Arthrogenic Muscle Inhibition, Knee Injuries, Postoperative Rehabilitation
- Trial name
- BIOQUAD (NCT07736625)
- Testing
- Visual Surface EMG Biofeedback, Standard Rehabilitation Without Visual Biofeedback
- Where
- France
- Volunteers
- 5 people
- Sponsor
- Hopitaux de Saint-Maurice
Obesity, Morbid, Bariatric Surgery Candidate
Comparison of the Effect of Traditional Method and Eras Protocol in Obesity Surgery
This study was conducted to compare the effectiveness of care based on the "Accelerated Recovery After Surgery (ERAS) Protocol" and the traditional method in bariatric surgery and demonstrate the difference the two methods based…
- Conditions
- Obesity, Morbid, Bariatric Surgery Candidate, Obesity Adult Onset, Obesity Associated Disorder
- Trial name
- NCT05790317
- Testing
- Surgical Procedure with ERAS Protocol
- Where
- Turkey (Türkiye)
- Volunteers
- 128 people, healthy volunteers welcome
- Sponsor
- Bahçeşehir University