Novosyn® Quick in Patients Undergoing Episiotomy Closure
NCT05233527 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 229
Last updated 2026-04-17
Summary
Retrospective, monocentric clinical study on the clinical performance of Novosyn® Quick in patients undergoing episiotomy closure.
Conditions
- Episiotomy Wound
Interventions
- PROCEDURE
-
Episiotomy Closure
indicated episiotomy with Novosyn® Quick after spontaneous vaginal delivery
Sponsors & Collaborators
-
B.Braun Surgical SA
collaborator INDUSTRY -
Aesculap AG
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-05-09
- Primary Completion
- 2026-03-26
- Completion
- 2026-10-31
Countries
- Spain
Study Locations
More Related Trials
-
Evaluation of the Modalities of Administration of Synthetic Oxytocin During Spontaneous Labor
NCT04935242 ·Status: COMPLETED
-
Comparison Between Two Medical Devices for Labor Induction After Previous C-section
NCT06506721 ·Status: RECRUITING ·Phase: NA
-
Cervical Ripening for Induction of Labor: Misoprostol Versus Oxytocin in Conjunction With Foley Balloon
NCT01139801 ·Status: COMPLETED ·Phase: NA
-
Chloroprocaine 3% - Epidural Anesthesia in Unplanned Caesarean Section
NCT02919072 ·Status: TERMINATED ·Phase: PHASE3
-
Comparison of the Effectiveness, Safety, and Satisfaction of Different Methods for Labor Induction
NCT06794385 ·Status: NOT_YET_RECRUITING ·Phase: PHASE4
-
Nitrous Oxide and Neuraxial Labor Analgesia Use on Maternal Fetal Outcomes
NCT04813874 ·Status: WITHDRAWN
-
A Combination of Antibiotics to Decrease Neonatal Morbidity and Mortality for Previable Threatened Labor
NCT06572761 ·Status: NOT_YET_RECRUITING ·Phase: PHASE3
-
Membrane Sweeping in Early Labor and Delivery Outcomes
NCT03517696 ·Status: WITHDRAWN ·Phase: NA
-
Outcomes Following Pre-marking of Episiotomy Location
NCT04719533 ·Status: UNKNOWN ·Phase: NA
-
Necessity of Antibiotics for Prevention of Delivery-associated Infections After Spontaneous Vaginal Delivery at Term
NCT02131818 ·Status: TERMINATED ·Phase: PHASE4
-
Concurrent Membrane Sweeping With Dinoprostone Versus Dinoprostone in Labor Induction of Nulliparas at Term With an Unfavorable Cervix
NCT01792375 ·Status: COMPLETED ·Phase: NA
-
Concurrent Oxytocin With Membrane Sweeping Versus Dinoprostone Pessary in Labor Induction of Multiparous Women at Term
NCT02618096 ·Status: COMPLETED ·Phase: NA
-
Cook Balloon Versus Propess After 12 Hours of Rupture of Membranes
NCT03310333 ·Status: UNKNOWN ·Phase: PHASE4
-
Vaginal Microbiome Seeding and Health Outcomes in Cesarean-delivered Neonates.
NCT03298334 ·Status: RECRUITING ·Phase: PHASE1/PHASE2
-
Verify the Safety and Effectiveness of the Cerclage Pessary in Prevention and Treatment of High-risk Preterm Pregnancy
NCT03637062 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Copper Intrauterine Device (IUD) Insertion at Cesarean Delivery
NCT01439802 ·Status: COMPLETED ·Phase: PHASE4
-
Cervical Ripening With Cook Catheter Plus Low Dose Oxytocin
NCT02465164 ·Status: COMPLETED ·Phase: NA
-
Induction of Labor in Pregnant Women With Prelabor Rupture of Membranes - Oxytocin or Misoprostol
NCT05215873 ·Status: COMPLETED ·Phase: PHASE4
-
Premature Rupture of Mambrane and Unfavourable Cervix
NCT01615107 ·Status: UNKNOWN ·Phase: NA
-
The Patient Positioning for Perineal Protection Study
NCT04616170 ·Status: COMPLETED ·Phase: NA
-
Management of Postoperative Pain After Cesarean Delivery Using Bridge Auricular Percutaneous Nerve Field Stimulator
NCT06434714 ·Status: WITHDRAWN ·Phase: NA
-
Nitrous Oxyde During Labour
NCT06595303 ·Status: COMPLETED
-
Feasibility Study to Evaluate the Role of a Novel Device in Childbirth
NCT05373342 ·Status: NOT_YET_RECRUITING
-
Lateral Episiotomy or Not in Vacuum Assisted Delivery in Non-parous Women
NCT02643108 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Double Balloon Catheter Versus Dinoprostone Vaginal Insert for Cervical Ripening.
NCT01170819 ·Status: COMPLETED ·Phase: PHASE4