Clinical trials: Polypropylene
Pelvic Organ Prolapse
Safety Study of Pelvic Organ Prolapse Repair Using Transvaginal Mesh
Pelvic organ prolapse is characterized by a lack of pelvic floor support causing the pelvic organs and vaginal walls to protrude.
- Trial name
- NCT00402844
- Testing
- Transvaginal mesh- PROLIFT®-system
- Where
- 26 sites in Denmark, Finland and 2 more
- Volunteers
- 250 people
- Sponsor
- Karolinska Institutet
Pelvic Organ Prolapse
RCT for Transvaginal Self-cut Mesh vs Mesh-kit for Severe POP
Pelvic organ prolapse(POP) is a common health problem and has significant negative effects on woman's quality of life. Transvaginal mesh procedure is a durable reconstructive surgery, but the mesh kits are expensive for…
- Trial name
- NCT03849157
- Testing
- pelvic floor reconstructive surgery
- Where
- 11 sites in China
- Volunteers
- 312 people
- Sponsor
- Peking Union Medical College Hospital
Pelvic Organ Prolapse
Flat Polypropylene Mesh in the Treatment of Uterine and Recurrent or Advanced Pelvic Organ Prolapse
This study is being done to evaluate the safety and feasibility of using flat polypropylene Restorelle® mesh, an ultra-lightweight mesh, for transvaginal use in surgically correcting certain specific cases of pelvic organ…
- Trial name
- NCT06225375
- Testing
- Restorelle® Flat Mesh
- Where
- United States
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- Michigan Institution of Women's Health PC
Neovascular Glaucoma
Comparative Study, Safety and Efficacy, Ahmed Glaucoma Drainage Device, Model M4 Model S2 in Neovascular Glaucoma
Objective: Prospectively evaluate the safety and efficacy of the Ahmed Glaucoma Drainage Device, model M4 compared with the model S2.
- Trial name
- NCT02260219
- Testing
- Surgical Implant of Ahmed Glaucoma Drainage Device, model M4 and S2
- Volunteers
- 42 people
- Sponsor
- Asociación para Evitar la Ceguera en México
Wound Vac, Suture
Wound Vac Polypropylene Suture Pilot Study
You are being asked to participate in this study because you have a complex wound that requires treatment with negative pressure wound therapy (NPWT).
- Trial name
- NCT02929238
- Testing
- Polypropylene Suture Right Side, Polypropylene Suture Left Side
- Where
- United States
- Volunteers
- 4 people
- Sponsor
- Prisma Health-Upstate
Pelvic Organ Prolapse
GYNEMESH PS Mesh Post Marketing Clinical Follow-Up Study
The objective of this retrospective and prospective, single-arm, observational, multicenter, post-market study is to evaluate outcomes in women who underwent surgery for vaginal or uterine prolapse with a GYNEMESH PS Mesh.
- Trial name
- NCT04829058
- Testing
- Intervention
- Where
- 3 sites in United States, Germany
- Volunteers
- 64 people
- Sponsor
- Ethicon, Inc.
Hernia
TIGR vs Polypropylene (Permanent) Mesh: Randomised Trial
Hypothesis: TIGR mesh as a reconstruction material is a more effective mesh for the repair of the abdominal wall post lipectomy, transverse rectus abdominis myocutaneous (TRAM) / deep inferior epigastric perforator (DIEP) flap.
- Trial name
- NCT01136603
- Testing
- TIGR Mesh
- Where
- Singapore
- Volunteers
- 80 people
- Sponsor
- National University Hospital, Singapore
Uterine Prolapse
Randomized Controlled Trial Comparing Acellular Collagen Biomesh (Pelvisoft) to Polypropylene Mesh(Pelvitex) for Sacral Colpopexy
This research protocol is a randomized controlled trial. It is being done to compare and find out the relative differences between the materials, (Pelivisoft) "natural organic mesh" to poly propylene mesh (Pelvitex) "manmade…
- Trial name
- NCT00564083
- Testing
- sacral colpopexy
- Where
- United States
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Atlantic Health System
Pregnancy, Cesarean Section
Comparison of Staples Versus Prolene Suture for Skin Closure at Cesarean Delivery
Currently different materials are used to close the skin after a cesarean delivery, including absorbable suture, non-absorbable suture and staples.
- Trial name
- NCT01509950
- Testing
- Staples, Prolene non-absorbable sutures, Absorbable Sutures
- Where
- United States
- Volunteers
- 15 people
- Sponsor
- Stanford University
Urinary Stress Incontinence
Comparative Study of PDVF and Polypropylene Transobturator Suburethral Tapes
This study evaluates the effectiveness and complications of polyvinylidene fluoride (PVDF) and polypropylene (PP) transobturator suburethral tapes (TOTs) in the treatment of female stress urinary incontinence.
- Trial name
- NCT02886520
- Testing
- PVDF transobturator tape, Polypropylene transobturator tape
- Where
- 9 sites in Spain
- Volunteers
- 286 people
- Sponsor
- Hospital Universitari Vall d'Hebron Research Institute
Inguinal Hernia
Is the Use of Prolene as Sufficient as the Use of Wire in Shouldice Surgery to Keep the Recurrence Rate Low After One Year?
When conducting the Shouldice procedure the 4-layer suture of the transversalis fascia is usually done with Prolene worldwide. At the Shouldice hospital the wire has originally been used for these augmentation.
- Trial name
- Wire vs Prolen (NCT05879770)
- Testing
- suture material
- Where
- Canada
- Volunteers
- 1,400 people, healthy volunteers welcome
- Sponsor
- Shouldice Hospital
Subluxation
A Novel Approach to Lens Subluxation
Evaluating new technique for treating patients with subluxation using specific laser type and new 6-0 proline fixating novel technique for the capsular bag
- Trial name
- NCT06773273
- Testing
- CapsuLaser-Assisted Capsulorhexis and Flanged Prolene Suture
- Where
- Saudi Arabia
- Volunteers
- 15 people
- Sponsor
- Zagazig University
Inguinal Hernia
Safety and Effectiveness of Optomesh 3D for Inguinal Hernia Repair
OPTIMUS is an observational study assessing the safety and effectiveness of Optomesh 3D, a shaped surgical mesh used in planned keyhole surgery for a groin (inguinal) hernia.
- Trial name
- OPTIMUS (NCT07836179)
- Testing
- Optomesh 3D
- Where
- Poland
- Volunteers
- 300 people
- Sponsor
- Swissmed Hospital
Hernia, Abdominal Hernia
Study of a New Laparoscopic Technique for Parastomal Hernia Repair With Mesh
The purpose of the study is to evaluate a new laparoscopic technique for parastomal hernia repair using an intraperitoneally placed Proceed mesh, looking at postoperative complications, recurrence rate and postoperative pain and…
- Trial name
- NCT00138957
- Testing
- Laparoscopic parastomal hernia repair with mesh
- Volunteers
- 20 people
- Sponsor
- University Hospital, Gentofte, Copenhagen
Breast Reconstruction After Mastectomy, Breast Neoplasm
Post Market Clinical Follow Up to "Patient Reported Outcome" Using a Titanised Polypropylene Mesh (TiLOOP® Bra Pocket)
"PRO-Pocket" - International prospective multicentre Post Market Clinical Follow Up to "Patient reported outcome" in primary or secondary breast reconstruction after mastectomy using a titanised polypropylene mesh (TiLOOP® Bra…
- Conditions
- Breast Reconstruction After Mastectomy, Breast Neoplasm, Breast Cancer, Breast Diseases
- Trial name
- PRO-Pocket (NCT03868514)
- Testing
- TiLOOP® Bra Pocket
- Where
- 12 sites in Austria, Germany
- Volunteers
- 313 people, healthy volunteers welcome
- Sponsor
- pfm medical gmbh