Clinical trials: Post Discharge
Lung Diseases
The Feasibility and Safety of Avoiding Chest Tube Placement After Video-assisted Thoracoscopic Surgery (VATS）of the Lung
This is a prospective randomized controlled trial.The main study content is the feasibility and safety of avoiding chest tube placement after Video-Assisted Thoracoscopic Surgery lung disease,participants were randomly divided…
- Trial name
- NCT04012554
- Testing
- avoid chest drainage tube placement after video-assisted thoracoscopic wedge resection of lung, Indewlling chest drainage tube after video-assisted thoracoscopic wedge resection of lung
- Where
- China
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Xueying Yang
Benign Prostatic Hyperplasia
A Study to Track the Safety of Vesomni in Men in South Korea Treated in Routine Clinical Practice for the Urinary Symptoms of Benign Prostatic Hyperplasia (Enlarged Prostate)
Benign prostatic hyperplasia (BPH), also known as an enlarged prostate, happens more often in men as they age. This condition causes a sudden need to pass urine, which is hard to control.
- Trial name
- NCT07619105
- Testing
- Vesomni
- Volunteers
- 600 people
- Sponsor
- Astellas Pharma Korea, Inc.
Blood Loss
Placental Cord Drainage After Vaginal Delivery
Placental Cord Drainage after Vaginal Delivery A randomized clinical trial
- Trial name
- NCT03487341
- Testing
- Cord drainage, Cord clamping
- Where
- Egypt
- Volunteers
- 600 people
- Sponsor
- Ain Shams University
Low Muscle Strength, Malnutrition
Efficacy of Oral Nutritional Supplement in Community-Dwelling Adults Following Acute Care
The study aims to determine the effects of Oral Nutritional Supplement (ONS) added to usual care on body weight compared with usual care alone in community-dwelling adults aged 55 years and older who are at risk of malnutrition…
- Trial name
- NCT07753239
- Testing
- ONS, Standard of Care (SOC)
- Where
- 7 sites in Thailand
- Volunteers
- 304 people
- Sponsor
- Abbott Nutrition
Post Procedural Infection
Assessing Dextenza Insert After SMILE Procedure
This three-month prospective, open-label, single-center, randomized investigator initiated clinical study seeks to investigate the efficacy of DEXTENZA when placed in the lower canaliculus (study eye) compared to topical…
- Trial name
- NCT04380857
- Testing
- Dexamethasone ophthalmic insert 0.4 mg, Topical Prednisolone Acetate Ophthalmic Drops
- Where
- United States
- Volunteers
- 20 people
- Sponsor
- William Wiley, MD
Transitions of Care, Patient Portals
Interactive Digital Health Tools to Improve Patient Safety in Acute Care
Study 1: The goal of this study is to implement and evaluate an interactive patient-centered discharge toolkit (PDTK) to engage patients and care partners in discharge preparation and communication with providers after discharge.
- Conditions
- Transitions of Care, Patient Portals, General Medicine, Discharge Checklist
- Trial name
- NCT03116074
- Testing
- Interactive Digital Health Tools
- Where
- United States
- Volunteers
- 750 people, healthy volunteers welcome
- Sponsor
- Brigham and Women's Hospital
Health Care Utilization, Nursing Caries
The Effect of Tele-Nursing on Parents of Circumcised Children
Circumcision is applied in many regions of the world for cultural, social, religious and medical reasons. Considering the frequency of circumcision in the World is 30%, this rate is close to 100% in Turkey.
- Trial name
- NCT05541913
- Testing
- Tele nursing
- Where
- Turkey (Türkiye)
- Volunteers
- 108 people, healthy volunteers welcome
- Sponsor
- Duzce University
Chronic Non Specific Low Back Pain
MFR Versus PFS Techniques on Pain,Range of Motion And Disability in Chronic Non Specific Low Back Pain.
To compare effect of myofascial Release versus post facilitation stretch in term of pain ,range of motion and disability in chronic non specific low back pain in patients.
- Trial name
- NCT05811260
- Testing
- Myofascial Release technique, Post facilitation stretch .
- Where
- Pakistan
- Volunteers
- 28 people
- Sponsor
- Riphah International University
Patients Returning Home After Discharge From Hospital
Sentinel Patients: Value of an Information System Collecting Patient's Own Report on His Healthcare Management
"Evolution of patient's health after hospital discharge is poorly documented. The investigators hypothesize that information of good quality on this concern might be accessible at a relatively low cost from patients, further…
- Trial name
- SENTIPAT (NCT01769261)
- Testing
- eligible, Internet, eligibles, telephone, non eligibles
- Where
- France
- Volunteers
- 2,090 people
- Sponsor
- Assistance Publique - Hôpitaux de Paris
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
Orthopaedic Related Pain (Musculoskeletal Pain), Opioid
Two Post-Operative Pain Protocols at Discharge for Orthopaedic Patients
This is a single-center, pilot randomized controlled trial designed to evaluate the feasibility of a definitive trial comparing opioid-free discharge prescriptions to usual care (which includes opioids) in patients undergoing…
- Conditions
- Orthopaedic Related Pain (Musculoskeletal Pain), Opioid, Pain, Pilot Study
- Trial name
- NCT07265557
- Testing
- Discharge pain medication prescription
- Where
- United States
- Volunteers
- 100 people
- Sponsor
- Massachusetts General Hospital
Coronary Artery Disease
Study Of Costs Realized After Percutaneous Coronary intervenTion Employing Same Day Discharge
The purpose of this study is to determine whether the total costs of care associated with uncomplicated elective or low-risk urgent percutaneous coronary intervention (PCI) through 30-day follow up are lower among patients who…
- Trial name
- SOCRATES (NCT02207270)
- Testing
- Same day discharge, Overnight Stay
- Where
- 2 sites in United States
- Volunteers
- 4 people
- Sponsor
- Trinity Health Michigan
Perianal Abscess, Anal Fistula
Antibiotics After Incision and Drainage to Prevent Fistula Formation After First Episode of Perianal Abscess
The goal of this clinical trial is to learn if antibiotics can prevent the formation of fistula-in-ano after incision and drainage of a first time of perianal abscess in adults.
- Trial name
- RAPID (NCT07704359)
- Testing
- Amoxicillin + Clavulanate, Ciprofloxacin + Metronidazole
- Where
- United States
- Volunteers
- 236 people
- Sponsor
- University of Illinois Chicago
Abdominal Drainage, Laparoscopic Cholecystectomy
Clinical Impact of Routine Abdominal Drainage After Laparoscopic Cholecystectomy
Patients and methods: 100 patients were included in this study. They divided into two groups, group (A) with drain and group (B) without drain.
- Conditions
- Abdominal Drainage, Laparoscopic Cholecystectomy, Gall Stones
- Trial name
- NCT00886210
- Testing
- intra abdominal drain, LC without drain
- Where
- Egypt
- Volunteers
- 100 people
- Sponsor
- Mansoura University
Chronic Postsurgical Pain
Effectiveness of Myofascial Release in Patients With Chronic Post Sternotomy Pain Syndrome
The main aim of this study is to investigate the effectiveness of Myofascial release in patients with chronic sternotomy pain.
- Trial name
- NCT06630208
- Testing
- Myofascial release, Breathing exercises, Pharmacological treatment
- Where
- Egypt
- Volunteers
- 60 people
- Sponsor
- Cairo University
Postoperative Nausea and Vomiting, Nausea and Vomiting, Postoperative
Post-Operative Nausea And Vomiting Study In Female Patients
The primary purpose of this study is to determine an effective dose of this NK-1 anti-emetic medication to prevent nausea and vomiting in females after surgery.
- Trial name
- NCT00274690
- Testing
- GW679769
- Where
- 44 sites in United States, Denmark and 9 more
- Volunteers
- 435 people
- Sponsor
- GlaxoSmithKline
Adhesive Capsulitis
Comparison of PFS and ART in Adhesive Capsulitis in Diabetic Patients
To determine the technique that will have better effects in realigning the muscle kinematics and to normalize the muscle activity along with reducing muscle stiffness with mobilizations techniques
- Trial name
- NCT04561310
- Testing
- Post facilitation stretch, Active release technique
- Where
- Pakistan
- Volunteers
- 36 people
- Sponsor
- Riphah International University
Cervicogenic Headache
Comparison of the Eficacy of Mulligan Mobilization and Myofascial Release in Patients With Cervicogenic Headache
Cervicogenic headache (CBH) is defined as a headache caused by a disorder in the cervical spine, bones, discs, or soft tissue elements, which is also accompanied by neck pain.
- Trial name
- NCT07508410
- Testing
- Mulligan mobilization therapy, Myofascial release therapy, Exercise therapy
- Where
- Turkey (Türkiye)
- Volunteers
- 90 people
- Sponsor
- Konya Beyhekim Training and Research Hospital
Bile Duct Stricture Not Treatable by ERC
Value of Percutaneous Cholangioscopy After Placement of a Percutaneous Transhepatic Biliary Drainage
In a prospective study the investigators perform repeated cholangioscopies in all patients that received percutaneous transhepatic biliary drainage (PTBD) for a variety of malignant and benign diseases.
- Trial name
- NCT00942630
- Where
- Germany
- Volunteers
- 40 people
- Sponsor
- Hannover Medical School
Medication Review, Polypharmacy
Medication Review in Chronic Complex or Polymedicated Patients After Hospital Discharge.
The goal of this prospective multicentre clustered randomized controlled trial is to evaluate the effect on new hospitalization episodes of a multidisciplinary medication review in primary care patients with polypharmacy or…
- Conditions
- Medication Review, Polypharmacy, Disease, Chronic
- Trial name
- NCT05799430
- Testing
- Multidisciplinary medication review, Control group
- Where
- Spain
- Volunteers
- 372 people
- Sponsor
- Fundación Pública Andaluza para la gestión de la Investigación en Sevilla
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