Biological OviTex Versus Synthetic Graft in Robotic Prolapse Surgery
Recruiting
N/A
Interventional Study
Colorectal Disorders
Prolapse
Prolapse Rectal
Prolapse Genital
Prolapse Pelvic
Rectocele
Prolapse Uterus
Cystocele
Enterocele
Prolapse Bladder
Prolapse; Cervix
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 184 (estimated)
- Sponsor
- Meander Medical Center · Other
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About This Trial
This prospective study aims to assess the efficacy of the OviTex 1S permanent mesh in pelvic floor surgery in comparison with the current standard polypropylene mesh.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Indication for VMR or SCR set by the treating surgeon/gynecologist in accordance to the current guidelines on rectal and pelvic prolapse;
* Counselled for therapeutic options and given informed consent for VMR or SCR;
* Counselled for different types of mesh (OviTex or Prolene…
Contacts