Healthy Participants Clinical Trial
The scientific goal of this experiment is to evaluate the performances of our three-dimensional digital model by comparing its prediction computed from underwater data to posture observed during real weightlessness during parabolic flight.
Investigations description Throughout the experiment test subject will be safely attached to
a fixation mechanism at its center of gravity (hip). This mechanism comprises a climbing
harness connected to two lateral vertical guides by two magnetic connection plates at the
level of the hips. The test subject will lie down on the floor on a plate equipped with foam
pads to create a comfortable lying surface. This mechanism allows free postural movement in
microgravity phase and also supports the test subject´s lying position during 1,8g- phase.
At any stage of the experiment the test subject will be able to exit the fixation alone, by
using one hand only.
The harness can be moved vertically by a linear sliding system and springs in the vertical
guides. Springs will remain compressed during the 1g/2g-phase and lift the subject with the
reduction to microgravity.
At the beginning of the weightlessness phase of each parabola, the sliding system will push
participant's body up to about 30cm above the floor. After he has reached the free floating
position, he will be asked to perform a short effort (crouching or stretching) and then to
relax and stay still.
Once free floating, three video cameras with wide angle lenses will record body movements
from front, side and top view. By electronically synchronizing the cameras the produced
images can be used for three-dimensional analysis. Additionally three-dimensional force
sensors at the hip fixation will be used to evaluate the quality of microgravity provided
during the parabolic flight.
Experimental protocol Before flight subjects will be familiarized with the setup and the
protocol. For each flight day, 3 subjects will be studied. The procedure will be the same
for the 3 subjects and on all 3 days.
The subject rests calm at the bottom until microgravity phase starts. As described above a
spring forced linear sliding system will push his body mass up to about 300mm. After the
test subject has reached its free floating position without any contact to the surrounding
area (bottom), he will perform a short effort (crouching or stretching). From now on the
subject should relax and is not allowed to move his muscles intentionally. At the end of
microgravity phase, the sliding system will allow a soft landing on the foam pads.
;
Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05445440 -
A Study to Assess the Effects of BMS-986371 on the Drug Levels of Methotrexate in the Presence and Absence of Sulfasalazine
|
Phase 1 | |
Completed |
NCT03712540 -
An Investigational Study of Experimental Medication BMS-986278 Given With the Antibiotic Rifampin in Healthy Participants
|
Phase 1 | |
Completed |
NCT03649165 -
A Study to Evaluate Bioavailability and Food Effect of Selumetinib (AZD6244) in Healthy Male Participants
|
Phase 1 | |
Completed |
NCT05956002 -
A Study to Evaluate the Study Medication (Etrasimod) When Mixed With Food in Healthy Participants
|
Phase 1 | |
Completed |
NCT05539976 -
A Taste Assessment of Iberdomide and Mezigdomide in Healthy Participants
|
||
Withdrawn |
NCT04558216 -
Evaluation of Effect of Rifampin on the Pharmacokinetics of Vonoprazan in Healthy Participants
|
Phase 1 | |
Withdrawn |
NCT03007771 -
Magnetic Resonance-guided High-Intensity Focused Ultrasound (MR-HIFU) Used for Mild Hyperthermia
|
Phase 1 | |
Completed |
NCT06097390 -
A Research Study Looking at New Protein-based Tablets in Healthy Men - Oral Formulation III
|
Phase 1 | |
Completed |
NCT05546151 -
A Study to Assess the Safety and Tolerability of BMS-986322 in Healthy Participants of Japanese Descent
|
Phase 1 | |
Completed |
NCT05056246 -
Study of AMG 133 Administered Subcutaneously in Healthy Japanese and Caucasian Participants
|
Phase 1 | |
Completed |
NCT04390776 -
Bioequivalence Study of PF-06651600 Capsules Relative to Tablets and Estimation of Food Effect on Capsules.
|
Phase 1 | |
Completed |
NCT05074459 -
A Study in Healthy Adults Investigating Eptinezumab Produced by 2 Different Manufacturing Cell Lines
|
Phase 1 | |
Enrolling by invitation |
NCT06089109 -
Creating VIP Corps to Reduce Maternal Deaths
|
N/A | |
Completed |
NCT05996250 -
Tolerance of an Immersive Virtual Reality Task Evaluating the Spatial Memory of Elderly Subjects
|
N/A | |
Completed |
NCT03278080 -
Development of Assessment Method for Driving Ability Using Driving Simulator in Healthy Volunteers #1
|
N/A | |
Completed |
NCT05064800 -
PF-07321332/Ritonavir and Ritonavir on Dabigatran Study in Healthy Participants
|
Phase 1 | |
Completed |
NCT04471298 -
A Study of Qishenyiqi Dripping Pills in Healthy Participants
|
Phase 1 | |
Completed |
NCT04914936 -
A Study to Evaluate the One-way Interaction of Calcium Carbonate, Omeprazole, or Rifampin on ACP-196
|
Phase 1 | |
Completed |
NCT02882386 -
Amino Acid Kinetics in Blood After Consuming Different Milk Protein Supplements
|
N/A | |
Completed |
NCT01681186 -
A Study of LY2940680 in Healthy Participants
|
Phase 1 |