Clinical trials: sponsored by University Ghent
Healthy
Bioavailability Study of a New Pediatric Formulation of Zidovudine/Lamivudine in Adult Volunteers
Description: To investigate bioavailability of two anti-viral drugs (lamivudine and zidovudine) from a new oral formulation (trial formulation) especially designed for pediatric use.
- Trial name
- NCT00470041
- Testing
- administration of two anti-viral drugs (lamivudine and zidovudine) from a new oral formulation
- Where
- Belgium
- Volunteers
- 12 people, healthy volunteers welcome
- Sponsor
- University Ghent
Malaria
Investigation of the Efficacy of Quinine Sulphate Administered Via Taste-Masked Pellets to Children With Falciparum Malaria
No pediatric formulations of quinine exist. Therefore, quinine tablets are broken into 2 or 4 parts, according to the body weight. Based on the body weight, 1/2 or 1/4 a tablet is administered to the child.
- Trial name
- NCT00329134
- Testing
- Administration of quinine sulphate taste-masked pellets
- Where
- Rwanda
- Volunteers
- 56 people
- Sponsor
- University Ghent
Postoperative Pain
The Prevention of Postoperative Epidural Catheter Migration: a Comparison of Three Types of Dressing
Three types of dressing will be compared to prevent postoperative epidural catheter migration. Patients will be randomised to have a Tegaderm dressing, an Epi-fix dressing or a Lockit-Plus dressing to secure the epidural catheter…
- Trial name
- NCT00764283
- Testing
- Tegaderm dressing, Epi-Fix dressing, Lockit-Plus
- Where
- Belgium
- Volunteers
- 200 people
- Sponsor
- University Ghent
Healthy
Study of the Effect of Lactisole on the Intestinal Glucose Uptake
Study of the effect of lactisole on glucose uptake
- Trial name
- NCT00631293
- Testing
- lactisole
- Where
- Belgium
- Volunteers
- 10 people, healthy volunteers welcome
- Sponsor
- University Ghent
Pressure Ulcer Lesions (Grade 2 or More)
Effectivity and Efficiency of Turning Frequencies: a Randomised Controlled Trial
Evaluation of the difference in pressure ulcer incidence or the time to develop pressure ulcers depending on the turning frequencies.
- Trial name
- NCT00262444
- Testing
- Different turning frequencies
- Where
- Belgium
- Volunteers
- 500 people
- Sponsor
- University Ghent
Scabies
Comparison of the Efficacy and Safety of Ivermectin to Permethrin
Comparison of the efficacy and safety of a single administration of ivermectin to a single administration of permethrin for the treatment of scabies
- Trial name
- NCT00262418
- Testing
- Administration of ivermectin or permethrin
- Where
- Belgium
- Volunteers
- 160 people
- Sponsor
- University Ghent
Healthy
The Effect of Wearing the 'Nike Free'Shoe on Isokinetic Muscle Strength of Foot and Ankle and on Proprioception.
To evaluate the effect of wearing the 'Nike Free'Shoe on isokinetic muscle strength of foot and ankle and on proprioception the following protocol will be used.
- Trial name
- NCT00389662
- Testing
- Wearing the "Nike Free" shoe
- Where
- Belgium
- Volunteers
- 45 people, healthy volunteers welcome
- Sponsor
- University Ghent
Asthma
Pharmaceutical Care for Asthma Control Improvement (PHARMACI)-Study
The objective of this study is to evaluate the therapeutic effectiveness and cost-effectivity of pharmaceutical care for asthma patients.
- Trial name
- NCT00263159
- Testing
- Pharmaceutical care for asthma patients
- Where
- Belgium
- Volunteers
- 221 people
- Sponsor
- University Ghent
Diabetes Mellitus
Pharmaceutical Care for Diabetes Type 2 Patients: a Randomised Controlled Trial
The objective of this study is to evaluate the therapeutic effectiveness and cost-effectivity of pharmaceutical care for diabetes type 2 patients.
- Trial name
- NCT00277732
- Testing
- Pharmaceutical care at baseline and follow-up visits over 6 months
- Where
- Belgium
- Volunteers
- 288 people
- Sponsor
- University Ghent
CABG-Patients
Changes in Cerebrovascular Reactivity During Cognitive Activation After Cardiopulmonary Bypass: Relation With Intraoperative Embolic Load and Postoperative Neuropsychological Dysfunctions
The study aims to evaluate neuropsychological disorders in CABG patients. Measurements are performed 1 day before, 6 days, 6 months and 3-5 years after the surgery.
- Trial name
- NCT00394108
- Testing
- Determination of neuropsychological status
- Where
- Belgium
- Volunteers
- 66 people
- Sponsor
- University Ghent