Clinical trials: Ambulatory Care
Akut Kidney Injury, Renal Replacement Therapy for Acute Kidney Injury in ICU
The Role of Renal Resistive Index (RI) in Predicting Acute Kidney Injury Progression in Intensive Care Clinic
Acute kidney injury(AKI) is defined in the KDIGO guidelines as a ≥0.3 mg/dL (≥26.5 micromol/L) increase in serum creatinine in the previous 48 hours or a ≥1.5-fold increase in serum creatinine from baseline, known or presumed to…
- Trial name
- NCT06995222
- Testing
- renal resistive index with Doppler ultrasound
- Where
- Turkey (Türkiye)
- Volunteers
- 120 people
- Sponsor
- Gulhane Training and Research Hospital
Phantom Limb Syndrome With Pain
Clinical Trial Exploring the Outpatient Treatment of Phantom Limb Pain With Ketamine Administration in a Six Month Study With a Minimum Remission Period of 7 Days Between Treatment Session. 25-30 Subjects With an Ongoing History of Significant PLP.--FDA and IRB Approved.
Must be living Within a 50 mile radius of our study sites: Bay Area, Los Angeles, Albuquerque, Sacramento, Los Angeles An anecdotal report with administration of ketamine in a non-clinical setting providing and sustained…
- Trial name
- PLP (NCT07276542)
- Testing
- IM ketamine in dose finding and then continuation
- Where
- 4 sites in United States
- Volunteers
- 30 people
- Sponsor
- The Ketamine Research Foundation
Diabetes Mellitus, Type 2
Impact of Pharmacy Clinic on Diabetes Management
The Beaumont Hospital Royal Oak Outpatient Clinic (and other listed Beaumont recruiting locations) care for over 900 patients with diabetes.
- Trial name
- PharmaMD (NCT03377127)
- Testing
- Pharmacy Managed Diabetes Clinic (PMDC), Standard of Care (SOC)
- Where
- 4 sites in United States
- Volunteers
- 86 people
- Sponsor
- Corewell Health East
Hemorrhoids
HET Bipolar System: Validation of Outpatient Hemorrhoid Treatment
Purpose: The current study aims to evaluate the safety and effectiveness of the HET™ Bipolar System (Medtronic, Boulder, CO) for the treatment of grade I-II hemorrhoids in a prospective pilot study.
- Trial name
- HET (NCT02773420)
- Testing
- HET Application
- Where
- United States
- Volunteers
- 35 people
- Sponsor
- University of Illinois Chicago
Patient Safety, Manipulation, Spinal
(MIST2)-Part2: AEs Following DC Care at DC Teaching Clinic: Electronic
This study aims to compare different ways to establish severity from patients reporting a new or worsening symptom (adverse event) following a chiropractic treatment at a teaching clinic using an electronic platform.
- Trial name
- MIST2 (NCT03412110)
- Testing
- active surveillance: electronic platform
- Where
- United States
- Volunteers
- 416 people, healthy volunteers welcome
- Sponsor
- Parker University
Postpartum, Pregnancy Related
Postpartum Care Timing: A Randomized Trial
The purpose of this study is to determine if shortening the time to initial postpartum visit from six weeks to two weeks can improve clinic visit attendance and decrease usage of the emergency department.
- Trial name
- PUnCTuAL (NCT03733405)
- Testing
- Postpartum Visit at 6 Weeks, Postpartum Visit at 2 Weeks
- Where
- United States
- Volunteers
- 256 people, healthy volunteers welcome
- Sponsor
- University of California, Los Angeles
Endocarditis, Infective
Ampicillin and Ceftriaxone for the Treatment of Enterococcus Faecalis Infective Endocarditis.
Phase IV, open-label, randomized and multicenter clinical trial to prove that patients with Enterococcus faecalis infective endocarditis treated with an antibiotic treatment as a continuous infusion is non-inferior to the…
- Trial name
- DOBLEI (NCT06423898)
- Testing
- Ampicillin plus ceftriaxone in continuous infusion, Ampicillin plus ceftriaxone in intermittent infusion of 14 days, after which the treatment may be changed
- Where
- 18 sites in Spain
- Volunteers
- 284 people
- Sponsor
- Fundación Pública Andaluza para la gestión de la Investigación en Sevilla
COVID-19
Camostat Efficacy vs. Placebo for Outpatient Treatment of COVID-19 (CAMELOT)
This is a randomized, double-blind, placebo-controlled study of camostat mesilate in ambulatory patients with confirmed COVID-19 with at least one risk factor for severe illness.
- Trial name
- NCT04583592
- Testing
- Camostat Mesilate
- Where
- 21 sites in United States
- Volunteers
- 295 people
- Sponsor
- Sagent Pharmaceuticals Inc.
Colorectal Surgery
Clinical and Economical Evaluation of Colorectal Surgery in Ambulatory Care
Enhanced recovery after surgery (ERAS) significantly decreases mortality, morbidity and hospital length of stay without increasing the rate of re-hospitalization.
- Trial name
- Colon-Ambu (NCT03760939)
- Testing
- Clinical and economical evaluation
- Where
- France
- Volunteers
- 5 people
- Sponsor
- IHU Strasbourg
Interstitial Lung Disease (ILD), Fibrotic Interstitial Lung Disease
Optimizing the Follow-Up Journey in Interstitial Lung Disease: The OPTIMIZE-ILD-2 Trial
The OPTIMIZE-ILD-2 trial is a prospective, randomized, open-label clinical trial designed to evaluate the impact of a coordinated follow-up pathway on patients with established interstitial lung disease (ILD).
- Conditions
- Interstitial Lung Disease (ILD), Fibrotic Interstitial Lung Disease, Idiopathic Pulmonary Fibrosis (IPF), Progressive Pulmonary Fibrosis
- Trial name
- OPTIMIZE-ILD-2 (NCT07486206)
- Testing
- Standard ILD Follow-Up Pathway, Optimized One-Day ILD Follow-Up Circuit
- Where
- Spain
- Volunteers
- 152 people
- Sponsor
- Hospital de Granollers
Migraine Headache
Effectiveness of Education and Relaxation Program on Migraine Related Disability in Patients Attending Headache Clinic
Migraine causes severe impairment in quality of life (QOL) both during and between attacks. Migraine also increases absenteeism, reduces productivity at work as well as at home, disrupts social and family relationships, also is…
- Trial name
- NCT05039996
- Testing
- education and relaxation program
- Where
- Egypt
- Volunteers
- 60 people
- Sponsor
- Ain Shams University
Pulmonary Embolism
Electronic Support for Pulmonary Embolism Emergency Disposition
To evaluate the impact of an integrated electronic clinical decision support system to facilitate risk stratification and site-of-care decision-making for patients with acute pulmonary embolism.
- Trial name
- eSPEED (NCT03601676)
- Testing
- Integration of electronic clinical decision support
- Where
- 14 sites in United States
- Volunteers
- 1,703 people
- Sponsor
- Kaiser Permanente
Myoma;Uterus, Polyp Uterus
Paracervical Block Versus Transcervical Block in Outpatient Procedural Hysteroscopy
Hysteroscopy is a minimally invasive, diagnostic and therapeutic gynecological surgical technique and the gold standard in the study of the uterine cavity.
- Trial name
- NCT05967936
- Testing
- Bupivacaine Injection
- Where
- Canada
- Volunteers
- 242 people
- Sponsor
- Ciusss de L'Est de l'Île de Montréal
Pneumonia, Bacterial
Study Evaluating Streptococcus Pneumoniae Serotype Carriage Rate for Nasopharyngeal Carriage in Filipino Children
Evaluation of the carriage rate of Streptococcus pneumoniae in the nasopharynx of healthy children and the carriage rate and distribution of Streptococcus pneumoniae serotypes
- Trial name
- NCT00724828
- Volunteers
- 500 people, healthy volunteers welcome
- Sponsor
- Wyeth is now a wholly owned subsidiary of Pfizer
Substance Abuse
Brief Interventions for Drop-out Re-engagement
We will evaluate a series of interventions intended to help individuals who drop out of substance abuse treatment re-engage in order to improve treatment outcome.
- Trial name
- NCT00350571
- Testing
- brief (behavioral therapy), Drop out re-engagement motivational intervention, standard care follow up
- Where
- 2 sites in United States
- Volunteers
- 299 people
- Sponsor
- Yale University
Health Status Measures, Outcomes
Ambulatory Care Quality Improvement (ACQUIP)
Health care organizations, including the VA, are investing substantial effort to improve quality of care. As part of this process, greater emphasis is being placed on measurement of outcomes, and in particular, functional…
- Conditions
- Health Status Measures, Outcomes, Continuous Quality Improvement
- Trial name
- NCT00013130
- Testing
- Provision of health status information to patients provider
- Where
- 5 sites in United States
- Volunteers
- 62,487 people
- Sponsor
- US Department of Veterans Affairs
Staphylococcal Infection, Abscess
Comparison of Cephalexin Versus Clindamycin for Suspected CA-MRSA Skin Infections
The purpose of this study is to help define the role of antibiotics in the treatment of pediatric skin infections caused by community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA).
- Conditions
- Staphylococcal Infection, Abscess, Staphylococcal Skin Infection, Folliculitis
- Trial name
- NCT00352612
- Testing
- clindamycin, cephalexin
- Where
- United States
- Volunteers
- 200 people, healthy volunteers welcome
- Sponsor
- Aaron Chen
Post-Intensive Care Recovery
A Recovery-Oriented Counselling Group
The purpose of this study is to evaluate a recovery-oriented group counselling program for post-discharged critical illness survivors and their caregivers.
- Trial name
- NCT03925181
- Testing
- Counselling Group
- Where
- Canada
- Volunteers
- 17 people, healthy volunteers welcome
- Sponsor
- University of Calgary
Acute Pulmonary Embolism, Outpatient Treatment
Prospective Study for the Outpatient Treatment of Patients With Very Low Risk Acute Symptomatic Pulmonary Embolism.
Objectives: To evaluate the safety of outpatient treatment of patients with very low-risk pulmonary embolism (PE), and the satisfaction and quality of life of this management.
- Trial name
- TRAMTEP (NCT05852119)
- Testing
- Outpatient treatment with standard anticoagulant therapy
- Where
- 10 sites in Spain
- Volunteers
- 300 people
- Sponsor
- Clinica Universidad de Navarra, Universidad de Navarra
Pelvic Floor Disorders
Does Using a 'Virtual Clinic' in Urogynaecology Improve Patient Experience and Reduce Cost?
The purpose of this study is to assess the impact of using a virtual clinic which combines a web-based interactive questionnaire (ePAQ-PF) used in advance of clinic appointments in combination with a telephone consultation has on…
- Trial name
- NCT02176330
- Testing
- ePAQ-PF followed by a telephone consultation., ePAQ-PF followed by a face to face consultation
- Where
- United Kingdom
- Volunteers
- 195 people
- Sponsor
- University of Sheffield