Plantarflexion Reduces Urgency and Peak Detrusor Pressure in Patients With Detrusor Overactivity

Overactive Detrusor Clinical Trial

— DO  

Official title:

Plantarflexion Reduces Urgency and Peak Detrusor Pressure in Patients With Detrusor Overactivity

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01837654
• Other study ID #: 76/12
• Status: Completed
• Phase: N/A
• Start date: June 2012
• Est. completion date: August 2012

Study information

• Verified date: November 2018
• Source: Assaf-Harofeh Medical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to find out whether plantarflexion has an effect on the degree of urinary urgency and on the amplitude of detrusor contraction during filling cystometry in patients with detrusor overactivity (DO).

Description:

Patients with urodynamic DO will be included in this study. During urodynamics, the mean peak detrusor pressures of each contraction will be documented and compared. At the beginning of the 2nd or 3rd wave, patients will be asked to perform continuous plantar-flexion by pushing their tiptoes against the floor. Following each wave, patients will be asked to grade the severity of the urgency by a visual analogue scale

Recruitment information / eligibility

• Status: Completed
• Enrollment: 22
• Est. completion date: August 2012
• Est. primary completion date: August 2012
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

All patients with urodynamic detrusor overactivity

Exclusion Criteria:

Inability to perform plantarflexion due to mental or physical disability

Related Conditions & MeSH terms

• Overactive Detrusor
• Urinary Bladder, Overactive

Intervention

Behavioral:
• Plantarflexion 2nd wave
At the beginning of the 2nd wave, patients will be asked to perform continuous plantar-flexion by pushing their tiptoes against the floor.
• Plantarflexion - 3rd wave
At the beginning of the 3rd wave, patients will be asked to perform continuous plantar-flexion by pushing their tiptoes against the floor.

Locations

Country	Name	City	State
Israel	Assaf Harofe Medical Center	Be'er Ya'aqov

Sponsors (1)

Lead Sponsor	Collaborator
Assaf-Harofeh Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Mean Peak Detrusor Pressures	Mean peak detrusor pressures of each contraction	through test completion, an average of 10 minutes
Secondary	Severity of the Urgency by a 0-10 Visual Analogue Scale (VAS).	Following each wave, patients will be asked to grade the severity of the urgency by a 0 (minimum) to 10 (maximum) visual analogue scale (VAS).	through test completion, an average of 10 minutes