A Self-Administered Maneuver to Relieve Symptoms Suggestive of Benign Prostatic Hyperplasia



Status:Completed
Conditions:Hematology, Benign Prostate Hyperplasia, Urology
Therapuetic Areas:Hematology, Nephrology / Urology
Healthy:No
Age Range:45 - Any
Updated:4/21/2016
Start Date:May 2008
End Date:November 2009

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Study of a Self-Administered Maneuver to Initiate and Maintain Urine Flow Impeded by Benign Prostatic Hyperplasia

The objective of this study was to evaluate the effectiveness of the Digital Repetitive
Infrapubic Pressure maneuver, a self-administered procedure used to provide symptomatic
relief in initiating and maintaining urine flow impeded by benign prostatic hyperplasia.

Eligible patients were alternately assigned to either immediate instruction on the use of
the Digital Repetitive Infrapubic Pressure maneuver (immediate intervention group) or to a
return appointment to receive instructions in the maneuver four weeks after the initial
assessment date (delayed intervention group). Patients were to utilize the procedure on
every occasion they had difficulty initiating, maintaining, or completing urine flow between
the time of their instruction and their subsequent visit. At the initial assessment visits
and the final visit, the patients completed an International Prostate Score Sheet (IPSS). A
telephone survey was conducted with all patients an average of nine months following their
instruction in the maneuver, to determine the extent to which they were still using it.

Inclusion Criteria:

- mild to moderate symptoms of difficulty initiating and maintaining the flow of urine

- not currently receiving treatment for the condition

- not taking an alpha-blocker at least one month before randomization

- not taking 5-alpha reductase inhibitor six months or more before randomization.

Exclusion Criteria:

- non-ambulatory

- taking medications known to affect urination,

- any of the following: a debilitating concomitant illness, a history of prostate or
bladder cancer or prostate surgery or radiation treatment to the pelvis, urethral
stricture, neurogenic bladder, current urinary tract infection or otherwise
potentially compromised urinary tract systems, a creatinine level of over 3.0 mg per
deciliter, or a residual urinary volume after voiding of over 350 cubic centimeters.
We found this trial at
1
site
Santa Clara, California 95014
?
mi
from
Santa Clara, CA
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