LEAFix Adhesion in Healthy Volunteers
NCT05415059 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32
Last updated 2022-08-08
Summary
This study compares the adhesiveness of the 3M material to be used in the final design.
Conditions
- Adhesion
Interventions
- DEVICE
-
Covatech Stoma bag material
Strips of Covatech Stoma bag used to asses adhesion of 3M material to be used in LEAFix device
Sponsors & Collaborators
-
Liverpool University Hospitals NHS Foundation Trust
lead OTHER_GOV
Study Design
- Allocation
- NA
- Purpose
- BASIC_SCIENCE
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2022-08-10
- Primary Completion
- 2022-10-31
- Completion
- 2022-11-30
More Related Trials
-
A Clinical Comparison of Two Marketed Skin Barriers on Healthy Volunteers
NCT01534039 ·Status: COMPLETED ·Phase: PHASE4
-
Safety and Performance of Short- and Long-term Baseplates for Attaching the UNEEG Episight Recorder - Part II
NCT06934005 ·Status: COMPLETED ·Phase: NA
-
Investigation of New Intermittent Catheters in Healthy Volunteers
NCT04445051 ·Status: COMPLETED ·Phase: NA
-
Safety and Performance of Short- and Long-term Baseplates for Attaching the UNEEG Episight Recorder - Part I
NCT05111847 ·Status: COMPLETED ·Phase: NA
-
Study to Assess Adhesion Quality and Wear of Placebo JNJ-35685-AAA-G-023 Transdermal System in Healthy Adults
NCT02221726 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
Device to Reduce Surgery Site Contamination
NCT00972153 ·Status: COMPLETED ·Phase: NA
-
Gen 2 Battrode Wear Study
NCT07256951 ·Status: RECRUITING ·Phase: NA
-
Modality Augmentation for Navigation: Intuitive Fusion With Optical Lightweight Device (US/CBCT)
NCT03231046 ·Status: WITHDRAWN ·Phase: NA
-
A Device to Determine Return of Sensation From Spinal Block
NCT04553913 ·Status: COMPLETED ·Phase: NA
-
Medical Adhesive Repeat Application Study
NCT04869696 ·Status: COMPLETED
-
Effectiveness and Safety of CT-guided Needle Placement in the Liver With the Aid of the ActiSight Needle Guidance System
NCT01367392 ·Status: COMPLETED ·Phase: PHASE4
-
Open Label Trial to Evaluate the Adhesion of TK-254RX in Healthy Volunteers.
NCT06042192 ·Status: COMPLETED ·Phase: PHASE1
-
Characterization of the Plasma Proteome Following Left Ventricular Assist Device Implantation
NCT02428894 ·Status: COMPLETED
-
Testing the Efficacy and Safety of the WEI Nasal Jet
NCT02005406 ·Status: COMPLETED
-
An Assessment of the Zephyr BioPatch and Its Ability to Monitor Patient Position
NCT02548624 ·Status: WITHDRAWN
-
Assessing Pain and Effectiveness of Carevix Device for IUD Insertions
NCT07290517 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Response to an Investigational Device in Patients With Restless Legs Syndrome
NCT06866132 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
A Multi-Center Protocol for Obtaining and Storing Human Samples for Immediate or Future Microbial, Immune, or Host-Microbe Scientific Study
NCT00764023 ·Status: COMPLETED
-
Evaluation of the Safety and Effectiveness of ALLEVYN Gentle Border
NCT03877484 ·Status: COMPLETED
-
Clinical Investigation for New Filter to Ostomy Bags
NCT01273038 ·Status: COMPLETED ·Phase: NA
-
Proof of Concept Study for 1 Lead Patch Technology
NCT02533531 ·Status: TERMINATED ·Phase: NA
-
Prospective Healthy Volunteer Study of the Securis™ Stabilization Device
NCT04841330 ·Status: COMPLETED
-
CAVA: Electrode Pad Appraisal Trial
NCT04012515 ·Status: COMPLETED ·Phase: NA
-
Suction Cervical Stabilizer Compared to Standard Tenaculum for Intrauterine Procedures
NCT06193590 ·Status: COMPLETED ·Phase: NA
-
Clinical Application and Validation of Innovative Tourniquet
NCT05605990 ·Status: COMPLETED ·Phase: NA