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Innovative Taping Technique for Catheter Complications
Study Summary
This trial will assess the effectiveness of 3 taping methods to keep IVs from being pulled from the skin. 6 measurements per subject will be taken to measure resistance to force.
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- You have too much hair in the inner elbow area of your arm.You have allergies to adhesive materials.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
- Group 1: Retrograde Directional Test
- Group 2: 90 Degrees Directional Test
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Frequently Asked Questions
May I enroll in this clinical research program?
"A total of 35 adults aged 18-65 who have experienced a displaced catheter are required for this trial. Notably, applicants must be employed by Boston Children's Hospital to qualify."
Does this research trial accept participants over the age of eighty-five?
"According to the rules of this trial, 18 is the youngest age possible for participation and 65 marks the upper limit."
What opportunities are available for individuals to join the current clinical trial?
"Affirmative. According to clinicaltrials.gov, recruitment for this medical trial is still in progress and set to begin on July 28th 2023 with its last update occuring on August 9th of the same year. The experiment requires 35 participants from a single location."
What is the enrollment capacity for this medical experiment?
"Affirmative. Clinicaltrials.gov indicates that this trial, which was initially advertised on July 28th 2023, is presently recruiting prospective participants. 35 volunteers are needed from a single medical centre for the study to proceed."
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