Actively Recruiting
Quality of Life After Conservative and Surgical Treatment of Pelvic Organ Prolapse
Led by University Hospital, Basel, Switzerland · Updated on 2024-07-30
134
Participants Needed
1
Research Sites
13 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are observing people with Pelvic Organ Prolapse to gather baseline and follow-up information about their condition and quality of life. The study does not assign patients to any specific treatments but aims to collect data that will help improve future treatment methods for both conservative and surgical therapies. This observational study is sponsored by the University Hospital in Basel, Switzerland. Participants will be monitored over time without intervention from the study team. The main focus is to assess symptom changes using the German Pelvic Floor Questionnaire before treatment and for up to five years afterward. This allows researchers to understand how symptoms evolve after different treatment approaches. People taking part in the study will share information through questionnaires and clinical assessments at various times over the follow-up period. The study tracks symptom changes and quality of life related to Pelvic Organ Prolapse and associated conditions such as incontinence. Participation lasts up to five years, with regular evaluations to gather meaningful data about patient experiences and outcomes.
CONDITIONS
Brief Title
Quality of Life After Conservative and Surgical Treatment of Pelvic Organ Prolapse
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pelvic Organ Prolapse (POP)
You will not qualify if you...
- Younger than 18 years
- Unable to understand informed consent
- Unwilling to participate
- Emergency operations
- Pregnancy
- Overactive Bladder without descensus
- Stool incontinence without POP
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 5 years
Participants are observed over time to assess quality of life and symptom changes after conservative or surgical treatment of pelvic organ prolapse.
Trial Site Locations
Total: 1 location
1
University Hospital Basel/Dep. of Visceral Surgery (Clarunis)
Basel, Switzerland
Actively Recruiting
Research Team
D
Daniel C Steinemann, PD Dr. med.
S
Sebastian Christen
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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