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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03825653
Other study ID # P.T.REC/012/001885
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date January 29, 2019
Est. completion date February 2020

Study information

Verified date December 2018
Source Cairo University
Contact yara n zaki, M sc.
Phone 01010446044
Email ynz.yara@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study will be conducted to assess biomechanical alignment of lower limb as a predictor for the stress urinary incontinence in the postmenopausal women. 300 postmenopausual women will be selected suffering from stress unrinary incontinence . Their age ranges from 60 to 70 years old. Their BMI is not exceeding 30 kg/m2.


Description:

in this study 300 postmenopausual women will be selected suffering from stress unrinary incontinence. Their age ranges from 60 to 70 years old. Their BMI is not exceeding 30 kg/m2. different methods of assessment will be used as : Data recording sheet, Weight-Height scale, Goniometer ,x ray radiography ,Transabdominal ultrasound and Perineal ultrasound. Data recording sheet: It will be used to record data of each woman before starting this study. Weight-Height scale: It will be used to measure weight and height of each woman before starting this study. Goniometer: it will be used to document the initial and the subsequent range of motion for ankle joint for each woman. Transabdominal ultrasound: it will be used for measurement of Post-void residual volume PVR for each woman which is the volume of urine left in the bladder after micturition . Perineal ultrasound: it will be used to assess the posterior urethrovesical angle for each woman . X-ray radiography: lateral pelvic radiographs will be taken for each woman in order to objectify the individual pelvic tilt. Inclusion criteria include : Subjects will be postmenopausal women complaining from stress urinary incontinence Participants age will range from 60-70 years.Their BMI will not exceed 30 kg/m2. Exclusion criteria: previous history of cancer and radiotherapy, any disease that could interfere with the participation, lower urinary tract infections( Manshadi F. etal ) musculoskeletal problems; previous major abdominal or pelvic surgery; severe diseases; diabetes mellitus, a body mass index >30 kg/m2; intraureterine device implantation, pelvic organ prolapse and menopause (Cerruto M etal.)


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 300
Est. completion date February 2020
Est. primary completion date February 2020
Accepts healthy volunteers No
Gender Female
Age group 60 Years to 70 Years
Eligibility Inclusion Criteria:

Subjects will be 300 postmenopausal women suffering from stress urinary incontinence Participants age will range from 60-70 years.Their BMI will not exceed 30 kg/m2

Exclusion Criteria:

- previous history of cancer and radiotherapy, any disease that could interfere with the participation, lower urinary tract infections( Manshadi F. etal ) musculoskeletal problems; previous major abdominal or pelvic surgery; severe diseases; diabetes mellitus, a body mass index >30 kg/m2; intraureterine device implantation, pelvic organ prolapse and menopause (Cerruto M etal.)

Study Design


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Outcome

Type Measure Description Time frame Safety issue
Primary Post-void residual volume PVR Transabdominal ultrasound
it will be used for measurement of Post-void residual volume PVR for each woman which is the volume of urine left in the bladder after micturition
30 minutes for every patient
Primary posterior urethrovesical angle perineal ultrasound will be used to assesse the posterior urethrovesical angle for each woman 30 minutes for every patient
Primary pelvic tilt lateral pelvic radiographic xray will be taken for each woman in order to objectify the individual pelvic tilt 30 minutes for every patient
Secondary ankle range of motion goniometer will be used to measure the range of motion for ankle joint 10 minutes for every patient
Secondary BMI weight height scale will be used to measure weight and height of each woman before starting this study 10 minutes for every patient
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