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Be Part of Research - Trial Details - Solifenacin Succinate Versus Tolterodine 4mg Once Daily

Solifenacin Succinate Versus Tolterodine 4mg Once Daily

Completed

Open to: ALL

Age: 18.0 - N/A

Medical Conditions

Urinary Bladder, Overactive


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Prospective, double-blind, double-dummy, 2-arm, parallel-group, design. Flexible dose regimen for solifenacin succinate, fixed dose treatment regimen for tolterodine. Assessment of OAB symptoms by patient diaries.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Jul 2003 Oct 2004

Publications

"Chapple CR, Martinez-Garcia R, Selvaggi L, Toozs-Hobson P, Warnack W, Drogendijk T, Wright DM, Bolodeoku J; STAR study group. A comparison of the efficacy and tolerability of solifenacin succinate and extended release tolterodine at treating overactive bladder syndrome: results of the STAR trial. Eur Urol. 2005 Sep;48(3):464-70. doi: 10.1016/j.eururo.2005.05.015."; "15990220"

INTERVENTIONAL

Intervention Type : DRUG
Intervention Description : oral

Intervention Arm Group : I;

Intervention Type : DRUG
Intervention Description : Oral

Intervention Arm Group : II;



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Harrow
  • Birmingham
  • Liverpool
  • London
  • Plymouth
  • Sheffield
  • Swansea
  • Leicester
  • Stevenage


The study is sponsored by Astellas Pharma Inc




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Read full details for Trial ID: NCT00802373
Last updated 17 September 2014

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