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Hernia Surgery Urinary Retention

M

Memorial Health University Medical Center

Status and phase

Unknown
Phase 4

Conditions

Urinary Retention
Hernia

Treatments

Drug: Tamsulosin

Study type

Interventional

Funder types

Other

Identifiers

NCT03027115
MHUMC 2016.10.05

Details and patient eligibility

About

Investigating whether pre-operative treatment with a selective alpha1-adrenoceptor antagonist affects the likelihood of male patients developing post-operative urinary retention following hernia repair.

Full description

The purpose of this study will be to investigate whether pre-operative treatment with a selective alpha1-adrenoceptor antagonist affects the likelihood of male patients developing post-operative urinary retention following hernia repair surgery. It is also of interest to determine whether or not a well-known urological screening tool, the IPSS, can identify patients at risk for urinary retention following elective laparoscopic or open hernia repair surgery. We will investigate if it is possible to pre-treat patients with a selective alpha1-adrenoceptor antagonist which we think can reduce the incidence of post-operative urinary retention and the associated adverse consequences, especially in those patients at higher risk.

Enrollment

140 estimated patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male
  • 18 years of age
  • Presenting with hernia requiring surgical intervention

Exclusion criteria

  • Intolerability of tamsulosin or related drugs
  • Investigator discretion
  • Unwillingness or inability to comply with protocol procedures and assessments

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

140 participants in 2 patient groups

Treatment
Experimental group
Description:
treatment with a selective alpha1-adrenoceptor antagonist
Treatment:
Drug: Tamsulosin
Control
No Intervention group
Description:
no treatment

Trial contacts and locations

1

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Central trial contact

Vishu Danthuluri, M.D.; Andrew Schwemmer, M.D.

Data sourced from clinicaltrials.gov

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