Uterine Prolapse Clinical Trials

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Manchester Procedure Versus Vaginal Hysterectomy for Women With Uterine Prolapse: A Multi-Center Randomized Controlled Study (The Fin-UP Trial)

Status: Recruiting
Location: See all (6) locations...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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 the clinic at 2 and 5 years after the operation * fill in questionnaires at 1, 2, 5 and 10 years after the operation

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 100
Healthy Volunteers: f
View:

• 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. Patients with concurrent anterior or posterior compartment defects will be included.

Locations
Other Locations
Finland
Helsinki University Hospital
RECRUITING
Helsinki
Hospital Nova, The Wellbeing Services County of Central Finland
RECRUITING
Jyväskylä
Kuopio University Hospital
RECRUITING
Kuopio
Oulu University Hospital
RECRUITING
Oulu
Tampere University Hospital
RECRUITING
Tampere
Turku University Hospital
RECRUITING
Turku
Contact Information
Primary
Päivi K Karjalainen, MD, PhD
paivi.karjalainen@hyvaks.fi
+358142695512
Backup
Anniina Karioja, MD
anniina.karioja@pirha.fi
+358331165005
Time Frame
Start Date: 2026-05
Estimated Completion Date: 2041-12
Participants
Target number of participants: 426
Treatments
Experimental: The Manchester procedure
Active_comparator: Vaginal Hysterectomy
Related Therapeutic Areas
Sponsors
Collaborators: Oulu University Hospital, Helsinki University Central Hospital, Turku University Hospital, Hospital Nova, Central Finland, Kuopio University Hospital
Leads: Tampere University Hospital

This content was sourced from clinicaltrials.gov