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Round Procedure for Belly Button Surgery
Study Summary
This trial will compare five different ways to fix an umbilical hernia, and figure out which one works best.
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 a history of developing keloids (raised scars).You have had surgery to change the appearance of your belly button in the past.You are currently smoking cigarettes.You have a body mass index (BMI) of over 40, which indicates severe obesity.
- Group 1: Round Procedure
- Group 2: "Scarless" round procedure
- Group 3: "Inverted U" procedure
- Group 4: "Inverted V" procedure
- Group 5: Y deepithelialized" procedure
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- 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.
Frequently Asked Questions
What is the upper limit of individuals enrolled in this investigation?
"Verified. The clinicaltrials.gov website states that this study, which was initiated on the 1st of January 2016, is actively searching for participants. 175 individuals need to be enrolled from a single medical facility."
Can seniors aged 80 or above participate in this medical research?
"According to the trial's enrollment requisites, participants must be 18 years old or above and should not exceed 65 of age."
Are there opportunities for people to join this medical experiment currently?
"Correct. According to clinicaltrials.gov, this study is actively seeking participants as of June 1st 2022. The trial was originally posted on January 1st 2016 and needs 175 patients from one location."
Is it possible for me to enroll in this research project?
"175 subjects aged 18 to 65, who are undergoing umbilicoplasty, must meet the following eligibility criteria: Signed Informed Consent Form and female patients pursuing abdominoplasty or abdominal free tissue transfer (TRAM/DIEP flaps)."
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