Pelvic Organ Prolapse Clinical Trial
Official title:
Benefits of Peri-surgical Physical Therapy in the Management of III and IV Grades of Pelvic Organ Prolapse
NCT number | NCT02846480 |
Other study ID # | UAlcala_POP |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | June 2010 |
Est. completion date | June 2017 |
Verified date | February 2016 |
Source | University of Alcala |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
To find out the effectiveness of physical therapy associated with the surgical treatment over
the simptoms and quality of life in III and IV grades of pelvic organ prolapse, patients will
be randomly assigned to one of these groups: experimental group: pre-surgical and
post-surgical physical therapy + behavioral education + surgical therapy. Control group:
surgical treatment + behavioral education.
In both groups several physical therapy assessments will be undertaken: 1st before surgery;
2nd immediately after surgery; and after 6 weeks, 3th, 6th, 12th and 24th months
post-surgery.
Status | Completed |
Enrollment | 65 |
Est. completion date | June 2017 |
Est. primary completion date | December 2013 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Consecutive women diagnosed with grade III and IV pelvic organ prolapse, which would be operated for this reason at the Asturias Prince Hospital (Madrid-Spain). Exclusion Criteria: - Women diagnosed with different III / IV grade of POP or a history of conservative treatment not from the subproject "Physiotherapy in the POP grades I and II", or a history of POP surgery, or concurrent conditions that would be affect the treatment (neurological, gynecological or urological), or recurrent urinary infection or hematuria, or those III / IV grades in POP which is contraindicated or not possible to perform surgery. - Pregnant women or women with a vaginal birth in the last six months. - Women with cognitive limitations to understand the information, answer questionnaires, consent and / or participate in the study. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
BEATRIZ SANCHEZ SANCHEZ | Hospital Universitario Principe de Asturias, Instituto de Salud Carlos III |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The SF-12 Health Survey (SF-12) Spanish version | up to 24th months post-surgery. | ||
Primary | Assessment of pelvic floor muscles strength with Modified Oxford Scale and vaginal perineometry, vaginal dynamometry | up to 24th months post-surgery. | ||
Primary | International Consultation on Incontinences Short Form (ICIQ-SF) Spanish version. | up to 24th months post-surgery. | ||
Secondary | Urinary symptoms (urinary frequency, nocturia, urgency, incontinence, coital incontinence, nocturnal enuresis, frequency of urinary tract infections, dysuria and urinary difficulty). | up to 24th months post-surgery. |
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