Clinical trials: Follow-up
COVID-19, Fibrosis
Covid-19 Respiratory Sequelae French Cohort
As the investigators need data on long term outcome of Covid-19, especially respiratory sequelae, a national cohort is required.
- Conditions
- COVID-19, Fibrosis, Cohort, Follow-up
- Trial name
- PNEUMOCOVID (NCT05075785)
- Where
- France
- Volunteers
- 2,933 people
- Sponsor
- Centre Hospitalier Universitaire, Amiens
Smoking Cessation
Assessment of Safety and Efficacy of Varenicline in Patients That Wish to Stop Smoking
The primary objective of this protocol is to evaluate 12 weeks of treatment of varenicline compared to placebo for smoking cessation.
- Trial name
- NCT00594204
- Testing
- varenicline tartrate (CP-526, 555-18)
- Where
- 42 sites in Brazil, Colombia and 9 more
- Volunteers
- 593 people
- Sponsor
- Pfizer
Relapsing-remitting Multiple Sclerosis
Follow up Study of Patients on Fingolimod Who Were Enrolled in the Original Biobank Study (CFTY720DDE01)
The purpose of this single visit extension study is to explore immune status in RRMS patients treated for at least 48 months with fingolimod.
- Trial name
- NCT02720107
- Testing
- fingolimod
- Where
- 26 sites in Germany
- Volunteers
- 133 people
- Sponsor
- Novartis Pharmaceuticals
COVID-19
The Prognostic Factors of COVID-19 ARDS Patients and Their Long-term Follow-up of Pulmonary Function Test
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is an emerging infectious disease with high transmissibility. Around 20-25% of infected individuals develop severe COVID-19 disease requiring hospitalization and…
- Trial name
- NCT05490914
- Where
- Taiwan
- Volunteers
- 90 people, healthy volunteers welcome
- Sponsor
- National Taiwan University Hospital
Chronic Pain, Spasticity, Muscle
Medtronic PSR TDD PMCF
The purpose of this study is to provide continuing evaluation and reporting of safety and performance of the SynchroMed II Infusion System within its intended use. Data will support post-market surveillance obligations.
- Trial name
- NCT04714385
- Where
- 15 sites in Belgium, Czechia and 6 more
- Volunteers
- 209 people
- Sponsor
- Medtronic
Type 2 Diabetes, Telemedicine
Telemedicine Influence in the Follow up of the Type 2 Diabetes Patient
The purpose of this study is to evaluate the impact of a a real time teleassistance system in the clinical evolution of type 2 diabetic patients on self monitoring blood glucose in the Public National Primary Care System.
- Conditions
- Type 2 Diabetes, Telemedicine, Self Monitoring Blood Glucose, Primary Care
- Trial name
- NCT00527254
- Testing
- Telemedicine system
- Where
- Spain
- Volunteers
- 328 people
- Sponsor
- Province of Malaga Health Department
Relapsing-remitting Multiple Sclerosis
Efficacy, Safety and Tolerability of Atorvastatin 40 mg in Patients With Relapsing-remitting Multiple Sclerosis Treated With Interferon-beta-1b
The "SWiss Atorvastatin and Interferon-Beta 1b Trial In Multiple Sclerosis - Follow up Study" is the follow up study of the "SWiss Atorvastatin and Interferon Beta-1b Trial In Multiple Sclerosis (SWABIMS)" (see…
- Trial name
- NCT01111656
- Testing
- Interferon beta-1b group, Interferon beta-1b/Atorvastatin group
- Where
- Switzerland
- Volunteers
- 28 people
- Sponsor
- Insel Gruppe AG, University Hospital Bern
Major Depressive Disorder
Long-Term Follow Up Study
The LTFU study will conduct a naturalistic follow up of the well characterized CAN-BIND study population of patients every six months and continuing over a five-year period.
- Trial name
- CAN-BIND LTFU (NCT02998762)
- Where
- 5 sites in Canada
- Volunteers
- 96 people
- Sponsor
- Sidney Kennedy
Head and Neck Cancers, Laryngeal Carcinoma
Telemedicine Follow-Up for Early Laryngeal Cancer: a Randomized Controlled Trial Comparing Care Close to Home Versus Standard of Care
The goal of this clinical trial is to evaluate whether Telemedicine follow-up is a satisfactory and safe alternative to traditional follow-up care for patients treated for early glottic (vocal cord) cancer, particularly those who…
- Trial name
- Telemedicine (NCT06940505)
- Testing
- Telemedicine Follow-up
- Where
- Netherlands
- Volunteers
- 140 people
- Sponsor
- University Medical Center Groningen
Cancer, Lung, Radiotherapy; Complications
Follow-up of Pulmonary Radiotoxicity for Bronchopulmonary Cancer.
assess the consequences of low doses of radiation delivered by the volumetric radiotherapy, on the respiratory capacity of patients treated for bronchopulmonary carcinoma, by a follow up of functional respiratory exploration.
- Trial name
- TEFRARC (NCT03931356)
- Testing
- Pulmonary function tests
- Where
- France
- Volunteers
- 39 people
- Sponsor
- University Hospital, Brest
Infant, Small for Gestational Age
Follow-up to Adult Height of a Cohort of Subjects Born Small for the Gestational Age and Treated With Growth Hormone
This non-interventional study for prospective follow up of a cohort of 220 subjects born small for gestational age (SGA) is planned for the purpose of finding out if normalisation of adult height is associated or not with…
- Trial name
- SGA (NCT01196156)
- Where
- 28 sites in Spain
- Volunteers
- 443 people
- Sponsor
- Merck KGaA, Darmstadt, Germany
Chronic Sinus Disease
BREATHE Long-Term Follow-Up Study
This is a long-term follow-up of patients that participated in the BREATHE I study.
- Trial name
- NCT01319305
- Testing
- FinESS Sinus Treatment
- Where
- United States
- Volunteers
- 70 people
- Sponsor
- Entellus Medical, Inc.
Atopy, Asthma
Vitamin A Supplementation at Birth and Atopy in Childhood
INTRODUCTION Eight trials studying the effect of providing neonatal vitamin A supplementation (NVAS) have been reported, and another four are underway to test whether NVAS should become WHO policy.
- Conditions
- Atopy, Asthma, Eczema, Food Allergy
- Trial name
- NCT01779180
- Where
- Guinea-Bissau
- Volunteers
- 2,000 people
- Sponsor
- Bandim Health Project
Periodontitis
10 Year Follow up of RCT Comparing Different Regenerative Regenerative Procedures
Evaluate the 10-year stability clinical, radiographic outcomes obtained with the application of the modified minimally invasive surgery to deep pockets associated with intrabony defects.
- Trial name
- NCT05225142
- Testing
- Modified minimally invasive surgery, Modified minimally invasive surgery with enamel matrix derivative, Modified minimally invasive surgery with enamel matrix derivative and bone replacement graft
- Where
- Italy
- Volunteers
- 45 people
- Sponsor
- The European Research Group on Periodontology (ERGOPerio)
Osteoarthritis, Hip, Rheumatoid Arthritis
Exception Cementless Hip Stem
This study is a multicenter, retrospective and prospective, non-controlled, non-randomized post market clinical follow-up study.
- Conditions
- Osteoarthritis, Hip, Rheumatoid Arthritis, Inflammatory Arthritis, Congenital Hip Dysplasia
- Trial name
- Exception (NCT04349046)
- Testing
- Total hip arthoplasty (THA)
- Where
- 6 sites in Belgium, France
- Volunteers
- 332 people
- Sponsor
- Zimmer Biomet
Infant Showing No Response to Resuscitation
MedNav: Improving Neonatal Life Support (NLS)
This study was designed to evaluate if MedNav impacts the ability of novice resuscitators to perform Neonatal Life Support (NLS) in the simulated environment, and if this ability is maintained after a 7 week period.
- Trial name
- NCT02932683
- Testing
- MedNav
- Where
- United Kingdom
- Volunteers
- 41 people, healthy volunteers welcome
- Sponsor
- Chelsea and Westminster NHS Foundation Trust
Uric Acid Serum
A Prospective Cohort Study of China Serum Uric Acid Levels
Uric acid is the final breakdown product of purine degradation in humans. The association between high serum uric acid levels and arterial stiffness as well as endothelial dysfunction has been demonstrated in humans and uric acid…
- Trial name
- ASSURE (NCT03616769)
- Testing
- antiplatelet drugs ,statins ,antihypertensive drugs
- Volunteers
- 3,535 people
- Sponsor
- Shanghai 10th People's Hospital
Hernia
A Retrospective Study With Prospective Follow-Up of Laparoscopic Ventral Hernia Repair Utilizing the Bard Sepramesh IP Composite
This study will enroll subjects who underwent a laparoscopic ventral hernia repair utilizing Sepramesh at least 12 months before starting in this study.
- Trial name
- Sepramesh (NCT01305473)
- Where
- United States
- Volunteers
- 90 people
- Sponsor
- C. R. Bard
Deformity of Face
Postoperative Follow up After Head and Face Reconstructive Surgeries
In this observational follow-up study, patients with type III-IV head and face soft tissue deformities/defects following reconstructive surgeries will be asked to fill out 3 questionnaires, either through phone calls or video…
- Trial name
- NCT04405687
- Testing
- Severe head and face deformity reconstructive surgery
- Where
- China
- Volunteers
- 50 people
- Sponsor
- Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
Kidney Failure, Chronic, Disorders Associated With Peritoneal Dialysis
Effect of Glucose Degradation Products (GDP) on Endothelial Dysfunction
The purpose of this study is to evaluate the effects of neutral pH and low glucose degradation product (GDP)-containing peritoneal dialysis fluid (PDF) on systemic inflammation and endothelial dysfunction markers in incident PD…
- Trial name
- NCT01315314
- Testing
- Balance, Fresenius Medical Care, Germany
- Where
- South Korea
- Volunteers
- 146 people
- Sponsor
- Kyungpook National University Hospital
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