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Completed Phase 1 Interventional Accepts healthy volunteers

Pharmacologic Effects of Darifenacin and Tolterodine on Cardiovascular Parameters in Healthy Subjects

ClinicalTrials.gov ID: NCT00703703

Public ClinicalTrials.gov record NCT00703703. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 6:15 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A 3-way Cross-over, Randomized, Placebo-controlled, Double-blind, Multicenter Study to Assess Pharmacologic Effects of a 7-day Exposure to Darifenacin 15 mg o.d. and Tolterodine ER 4 mg o.d. on Cardiovascular Parameters in Healthy Subjects 50 Years of Age and Older

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will evaluate the pharmacologic effects of exposure to darifenacin and tolterodine on cardiovascular parameters in healthy subjects 50 years of age and older

Study identification

NCT ID
NCT00703703
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Novartis
Industry
Enrollment
117 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
50 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 2008 (Type not available)
Primary completion
Oct 2008 (Actual)
Completion
Oct 2008 (Actual)
Last update posted
Aug 2, 2012

2008

United States locations

U.S. sites
21
U.S. states
14
U.S. cities
21
Facility City State ZIP Site status
Investigative Site Phoenix Arizona — —
Investigative Site Tempe Arizona — —
Investigative Site Little Rock Arkansas — —
Investigative Site San Diego California — —
Investigative Site Washington D.C. District of Columbia — —
Investigative Site Fort Myers Florida — —
Investigative Site Jacksonville Florida — —
Investigative Site Jupiter Florida — —
Investigative Site Miami Florida — —
Investigative Site Orlando Florida — —
Investigative Site Overland Park Kansas — —
Investigative Site Topeka Kansas — —
Investigative Site Riverdale Maryland — —
Investigative Site Wellesley Hills Massachusetts — —
Investigative Site Springfield Missouri — —
Investigative Site Hackensack New Jersey — —
Investigative Site Burlington North Carolina — —
Investigative Site Greensboro North Carolina — —
Investigative Site Oklahoma City Oklahoma — —
Investigative Site Knoxville Tennessee — —
Investigative Site Morgantown West Virginia — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00703703, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 2, 2012 · Synced Oct 20, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00703703 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →