Novosyn® Quick in Patients Undergoing Episiotomy Closure
Spain229 participantsStarted 2024-05-09
Plain-language summary
Retrospective, monocentric clinical study on the clinical performance of Novosyn® Quick in patients undergoing episiotomy closure.
Who can participate
Age range
18 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Women who underwent an indicated episiotomy between January 2020 - December 2020 at the Hospital General de Catalunya (Sant Cugat del Vallès, Spain) and received Novosyn® Quick
Exclusion Criteria:
* No exclusion criteria have been set
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1This trial is comparing suture materials for closing an episiotomy wound — can you explain what makes Novosyn Quick different from the sutures you'd normally use, and why that difference matters for how my wound heals?
2The trial is specifically measuring wound dehiscence, which means the wound reopening — how common is that complication with standard episiotomy closure, and what would it mean for my recovery if it happened?
3Since this trial is no longer actively recruiting, does that mean the results might be available soon, and could those findings change what suture material you'd recommend for my care right now?
4Episiotomy recovery can affect comfort, mobility, and daily life for weeks — regardless of whether I'm part of this trial, is there anything about the suture options being studied here that my care team would consider when planning my closure?
5Are there any known differences in pain, healing time, or infection risk between the types of sutures being evaluated in this study that would be worth weighing when deciding on my treatment?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.