The Finnish Uterine Prolapse Surgery Trial (The Fin-UP Trial)

Recruiting N/A Interventional Study
Uterine Prolapse Pelvic Organ Prolapse Vaginal Surgery Pelvic Organ Prolapse (POP)
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 – 100
Sex
Female
Study type
Interventional
Purpose
Treatment
Participants needed
426 (estimated)
Sponsor
Tampere University Hospital · Other
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial
The goal of this clinical trial is to compare the Manchester procedure and vaginal hysterectomy in treating patients with symptomatic uterine prolapse. The main question it aims to answer is: • What is the difference in the success rates at the the two year follow-up Participants will: * be randomized in either the Manchester procedure or vaginal hysterectomy group and operated as such * visit…
Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
Inclusion Criteria: * Fit for elective vaginal surgery according to standard preoperative assessment * Women aged over 18 years * No previous POP surgery * Symptomatic POP stage 2 or higher, with uterine descent of at least stage 2 (POP-Q point C ≥ minus 1) and with POP-Q point D ≤ minus 1. Patient…
Contacts

Päivi K Karjalainen, MD, PhD

+358142695512

paivi.karjalainen@hyvaks.fi

CONTACT

Anniina Karioja, MD

+358331165005

anniina.karioja@pirha.fi

CONTACT