ClinicalTrials.Veeva

Menu

Advanced Biomarker Assessment in Pelvic Organ Prolapse

Mayo Clinic logo

Mayo Clinic

Status

Completed

Conditions

Pelvic Organ Prolapse

Study type

Observational

Funder types

Other

Identifiers

NCT03642054
17-009172

Details and patient eligibility

About

This study will assess advanced biomarkers in patients with and without vaginal prolapse. Assessments will be directed at vaginal fibroblasts and adipose derived stem cells.

Full description

Vaginal biopsies and abdominal adipose harvest will be accomplished in patients undergoing vaginal hysterectomy for non-prolapse benign conditions (6) and pelvic organ prolapse (6). Samples of tissues will be divided and portions will be snap-frozen, placed into transport medium for subsequent tissue digestion, and receive paraffin processing. Cells in transport medium will be transported to the Mayo Collaborative Research building (lab of Dr. David Lott) for isolation of fibroblasts and adipose derived stem cells.

The other samples will be transported to the lab of Dr. Andre van Wijnen (RST) to isolate RNA and protein for mRNA, microRNA and additional protein analysis.

Isolated fibroblasts and ASC's from the lab of Dr. Lott (MCA) will be expanded and passaged 3-5 times. ASCs phenotype will be confirmed by flow cytometry. Cells lines will be duplicated and biobanked at the Mayo Clinic Rochester Biotrust and separately biobanked at the Arizona State University lab of scaffold collaborator, Dr. Stephen Massia. Additional frozen cell lines will transported to the lab of Dr. Andre van Wijnen for further processing. . All cells and materials will be used for testing and to advance the science of regenerative medicine. No biobanked cells or materials from this specific project will be used for any future intervention or treatment in humans.

Enrollment

18 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria-

  • Patients undergoing vaginal hysterectomy for non-prolapse benign conditions and pelvic organ prolapse
  • at least 18 years old
  • Mayo Clinic patient

Exclusion Criteria-

°Patients who have a history of a recognized classic connective tissue disease

Trial design

18 participants in 2 patient groups

Pelvic Organ Prolapse
Description:
Patients having vaginal hysterectomy who demonstrate grade III-IV uterovaginal prolapse.
Non Pelvic Organ Prolapse
Description:
Patients having vaginal hysterectomy who do not demonstrate uterovaginal prolapse.

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems