Clinical trials: Post Discharge
Sepsis
Reducing 30-Day Sepsis Readmissions: Impact of a Post Discharge Education Program
This study will advance the knowledge in the field by determining the effectiveness of discharge education regarding prevention of a new infection which is the highest cause of readmission for sepsis patient.
- Trial name
- NCT05602896
- Testing
- Sepsis education
- Sponsor
- Washington University School of Medicine
Stroke
Regaining Confidence After Stroke a Feasibility Randomised Controlled Trial
The Regaining Confidence after Stroke Course (RCAS) is a group therapy intervention to evaluate the feasibility of conducting a definitive trial, aimed to facilitate adjustment for people with stroke discharged from…
- Trial name
- RCAS (NCT03807284)
- Testing
- A group psychosocial course
- Volunteers
- 51 people, healthy volunteers welcome
- Sponsor
- University of Nottingham
Hematopoietic Stem Cell Transplantation, Malnutrition
Nutrition Intervention Among Stem Cell Recipients: Post Hospital Discharge
Chemotherapy conditioning, preceding Stem Cell Transplantation (SCT), has been associated with severe gastrointestinal toxicity, commonly compromising patients' food intake, nutritional status and functioning level.
- Trial name
- NCT02791347
- Testing
- Nutrition Intervention
- Where
- Lebanon
- Volunteers
- 52 people
- Sponsor
- American University of Beirut Medical Center
Acute Cholecystitis, Empyema
Drainage is Not Necessary Procedure After Laparoscopic Cholecystectomy Due to Severe Acute Cholecystitis
Laparoscopic cholecystectomy (LC) is the current preferred method of cholecystectomy. The role of routine drainage after LC to decrease postoperative morbidity is still an issue of considerable debate.
- Trial name
- NCT01625247
- Testing
- Surgical drainage
- Where
- South Korea
- Volunteers
- 162 people
- Sponsor
- Yonsei University
Ischemic Stroke
A Phase 2b Study of Dalfampridine 10mg Extended Release Tablet in Subjects With Chronic Deficits After Ischemic Stroke
This is a multi-center, safety and tolerability study in subjects with chronic stable sensorimotor deficits after ischemic stroke. It has been designed as a double-blind, placebo-controlled, 2-period crossover study.
- Trial name
- NCT01605825
- Where
- 20 sites in United States
- Volunteers
- 83 people
- Sponsor
- Acorda Therapeutics
Morbid Obesity in Cardiac Surgery Patients, Postoperative Respiratory Dysfunction
Prophylactic Use of APRV Before Extubation in Morbidly Obese Patients After Cardiac Surgery.
Morbidly obese patients undergoing open heart surgery are at increased risk of breathing problems after removal of the breathing tube due to reduced lung function and chest wall restriction following surgery.
- Conditions
- Morbid Obesity in Cardiac Surgery Patients, Postoperative Respiratory Dysfunction, Mechanical Ventilation Strategies
- Trial name
- APRV-OBESE-CS (NCT07409324)
- Testing
- Airway Pressure Release Ventilation (APRV), Conventional Lung-Protective Mechanical Ventilation
- Volunteers
- 180 people
- Sponsor
- Ain Shams University
Postoperative Pain
Safety and Effectiveness of Tramadex-OD After Knee Arthroscopy
Extended-release tramadol is indicated for the management of moderate to severe pain in adults who require around-the-clock treatment.
- Trial name
- NCT01024348
- Testing
- extended-release tramadol, paracetamol
- Where
- Israel
- Volunteers
- 100 people
- Sponsor
- Shaare Zedek Medical Center
Congestive Heart Failure, Angina Pectoris
Does Telephone Follow-up Improve Patients Satisfaction
Several studies have shown the importance of Telephone follow-up in reducing hospital readmissions for heart failure. Therefore, we aimed in this cohort to investigate whether telephone follow-up with patients discharged from the…
- Conditions
- Congestive Heart Failure, Angina Pectoris, Pneumonia, Urinary Tract Infection
- Trial name
- NCT00192738
- Where
- Israel
- Volunteers
- 400 people
- Sponsor
- Rambam Health Care Campus
Minimally Invasive Surgical Procedure, Hysterectomy
The Impact of Post-operative Voiding Trial on Length of Stay Following Laparoscopic Hysterectomy: A Prospective, Randomized Control Trial
The aim of this study is to investigate the impact of an active voiding trial compared to a passive voiding trial on time to discharge following a planned same day discharge laparoscopic hysterectomy.
- Conditions
- Minimally Invasive Surgical Procedure, Hysterectomy, Urinary Retention
- Trial name
- NCT04487600
- Testing
- Active voiding trial
- Volunteers
- 130 people, healthy volunteers welcome
- Sponsor
- Brigham and Women's Hospital
Stroke, Upper Extremity Hemiplegia
"Remind-to-move" for Promoting Upper Extremity Recovery in Patients With Stroke After Subacute Discharge
This is a multi-centered randomized controlled trial to investigate the effects of "Remind-to-Move" (RTM) using wearable devices at home for promoting upper extremity recovery in stroke patients after discharge from subacute…
- Trial name
- NCT02952677
- Testing
- Remind-to-move, Control
- Volunteers
- 84 people
- Sponsor
- The Hong Kong Polytechnic University
Disorder of Knee
Open-Label Study of Oxycodone/APAP to Treat Post-Operative Pain Following Arthroscopic Knee Surgery
This is a pilot trial using this product in patients for the management of pain after outpatient arthroscopic knee surgery. This is an open-label study and the two active ingredients are well known pharmacologic entities.
- Trial name
- NCT02391844
- Testing
- Oxycodone
- Where
- United States
- Volunteers
- 50 people
- Sponsor
- International Clinical Research Institute
Musculoskeletal Injury, Spinal Injuries
Predictive Models for Spine and Lower Extremity Injury After Discharge From Rehab
The purpose of this study is to develop algorithms that will help predict future injury and/or re-injury after being returned to duty from a musculoskeletal injury.
- Conditions
- Musculoskeletal Injury, Spinal Injuries, Leg Injuries
- Trial name
- MP3-RD (NCT02776930)
- Where
- 4 sites in United States
- Volunteers
- 480 people
- Sponsor
- Brooke Army Medical Center
Hip Fracture
Back to the Future: Bridging the Hospital to Home Continuum After Hip Fracture
The purpose of this study is to determine whether is is feasible and acceptable to deliver a telephone based coaching intervention compared with education alone in community dwelling older adults (age 60 and older) after a fall…
- Trial name
- B2F (NCT01930409)
- Testing
- Telephone Support and Coaching, Education Only
- Where
- Canada
- Volunteers
- 30 people
- Sponsor
- University of British Columbia
Postgastrectomy Syndrome
Effects of Active Release Technique (ART) on Pectoralis Minor Tightness in Post Mastectomy Women.
The aim of this research is to determine the Effects of Active Release Technique (ART) on pectoralis minor tightness in post mastectomy women.
- Trial name
- NCT05497869
- Testing
- active release group, active control group
- Where
- Pakistan
- Volunteers
- 60 people
- Sponsor
- Riphah International University
Severe Malaria, Severe Anemia
PDMC Implementation Trial in Kenya
The goal of this implementation trial is to evaluate at least two alternative delivery strategies and adherence support for malaria chemoprevention with dihydroartemisinin-piperaquine in the post-discharge management of children…
- Trial name
- PDMC-SL (NCT06624631)
- Testing
- SMS reminders; adherence support strategy a, Community Health Promoters (CHP) home visits; adherence support strategy b, No reminders; adherence support strategy c
- Where
- Kenya
- Volunteers
- 600 people
- Sponsor
- Liverpool School of Tropical Medicine
Acute Disease
A Virtual Ward to Reduce Readmissions After Hospital Discharge
The purpose of this study is to see whether a Virtual Ward reduces readmissions after hospital discharge.
- Trial name
- NCT01108172
- Testing
- Virtual Ward, Usual care
- Where
- 5 sites in Canada
- Volunteers
- 1,928 people
- Sponsor
- Unity Health Toronto
Post-traumatic Stress Disorder (PTSD), Current Significant Sleep Disturbances
Sleep Disturbances in Children and Adolescents With Post-traumatic Stress Disorder (PTSD): a Randomized Double-blind Placebo-controlled Trial to Investigate the Efficacy of Pediatric Prolonged-release Melatonin
Among the most sensitive and persistent symptoms of post-traumatic stress disorder (PTSD) in children are sleep disturbances in the insomnia spectrum (sleep onset disturbances, fragmented sleep with multiple nocturnal awakening…
- Trial name
- MelatoSomKids (NCT07418554)
- Testing
- pediatric, prolonged released melatonin
- Where
- France
- Volunteers
- 120 people
- Sponsor
- University Hospital, Strasbourg, France
Anterior Cruciate Ligament Reconstruction, Tranexamic Acid
Tranexamic Acid Injection With Different Drainage Clamping Time After Anterior Cruciate Ligament Reconstruction
Post-anterior cruciate ligament reconstruction (ACLR) hemarthrosis may result in increased pain thus delaying postoperative rehabilitation, which may eventually lead to arthrofibrosis and a functional deficit.
- Conditions
- Anterior Cruciate Ligament Reconstruction, Tranexamic Acid, Hemarthrosis, Knee
- Trial name
- NCT06280456
- Testing
- Tranexamic Acid Powder
- Where
- Taiwan
- Volunteers
- 150 people, healthy volunteers welcome
- Sponsor
- Taipei Veterans General Hospital, Taiwan
Fatigue
Fatigue One Year After ICU Discharge
The investigators contacted consecutive adult patients admitted to intensive care unit (ICU) and mechanically ventilated for at least 72 hours to invite them to an interview at hospital.
- Trial name
- NCT02684877
- Testing
- Questionnaire
- Volunteers
- 56 people
- Sponsor
- Università degli Studi di Ferrara
Pain, Obstetric
Efficacy of Extended-Release Liposomal Bupivacaine for Post-Partum Pain Management Following Obstetrical Laceration
We propose a prospective, randomized, single blinded trial with subjects recruited from the WRNMMC Labor and Delivery Unit to study post-partum efficacy of Exparel® for pain control in patients undergoing a vaginal delivery who…
- Trial name
- NCT03152877
- Testing
- Bupivacaine Liposome Injectable Product, 0.25% plain bupivacaine
- Where
- United States
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Walter Reed National Military Medical Center
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