Verzakkingsklachten in de huisartspraktijk: de effecten van bekkenfysiotherapie en pessariumbehandeling.
Recruiting
- Conditions
- Pelvic organ prolapseUrogenitale prolaps (Nederlands)
- Registration Number
- NL-OMON25669
- Lead Sponsor
- niversity Medical Center Groningen (UMCG), departments of general practice and epidemiology
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 366
Inclusion Criteria
1. Women older than 54 years;
2. Symptomatic stage I, II or III POP (pelvic organ prolapse quantification (POP-Q) );
Exclusion Criteria
1. Cognitive impairment (eg dementia);
2. Poor physical condition (according to their GP);
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pelvic Floor Distress Inventory (PFDI-20) score after 3, 12 and 24 months.
- Secondary Outcome Measures
Name Time Method 1. Global perception of improvement and VAS score of improvement of the symptoms after 3, 12 and 24 months;<br /><br>2. Pelvic Floor Impact Questionnaire (PFIQ-7) score, Pelvic organ prolapse / urinary incontinence sexual questionnaire (PISQ-12) score, MOS SF-12 score, EQ-5D score, after 3, 12 and 24 months;<br /><br>3. POP stage (POP-Q) after 3, 12 and 24 months;<br /><br>4. Costs of treatment;<br /><br>5. Number of women succesfully treated with a pessary;<br /><br>6. Number of women referred to a gynaecologist.