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Clinical study of solifenacin succinate in patients with bladder symptoms due to spinal cord injury or multiple sclerosis

This trial is complete
The study has ended normally, and participants are no longer being examined or treated (that is, the last participant's last visit has occurred).

Clinicaltrials.gov ID

The unique identification code given to each clinical study upon registration at ClinicalTrials.gov.
NCT00629642

Astellas Study ID

The unique identification code given by the study sponsor.

905-EC-005

EudraCT ID

The unique identification code given to each clinical study upon registration at EudraCT (European Union Drug Regulating Authorities Clinical Trials Database).

N/A

Follow Trial

Condition

Multiple Sclerosis, Bladder Disease, Spinal Cord Diseases

Phase

These clinical trials happen after a drug or treatment has been approved for patients to take. Clinical trials in phase 4 usually take place over many years because researchers want to learn about long term use and safety of a drug or treatment.

Phase 4

Age

18 years - 65 years

Sex

Female & Male

Product

N/A

Type

A type of clinical study in which participants are assigned to groups that receive one or more intervention/treatment (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.

Interventional

Trial Dates

Mar 2008 - Jan 2011

Masking

Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Enrollment number

249

A Randomized, Double Blind, Double Dummy, Placebo Controlled Study to Evaluate the Efficacy and Safety of Solifenacin Succinate (5 and 10mg once daily) against Placebo and Oxybutynin Hydrochloride (5 mg three times daily) in the Treatment of Subjects with Neurogenic Detrusor Overactivity

Study summary

Study documents

Study Documents, including study results, are available after a study is completed or terminated, according to Astellas Transparency policy.

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