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NCT00171470 · ClinicalTrials.gov registry record · Phase 3

The Role of Tegaserod Therapy in the Management of Dyspeptic Symptoms in Female Patients on Proton Pump Inhibitors for the Treatment of Heartburn.

A Phase 3 study of Dyspepsia, sponsored by Novartis.

Completed
Registry status
Phase 3
Development phase
60
Enrollment target
1
Study location

NCT00171470: Completed Phase 3 study of Dyspepsia, sponsored by Novartis.

NCT00171470 is a Phase 3 study of Dyspepsia that has completed, run by Novartis. The registered enrollment target is 60 participants, below the 71-participant average among 11 other Dyspepsia trials with a reported enrollment target (15% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00171470, a Phase 3 study of Dyspepsia, has completed, sponsored by Novartis.

COMPLETED
Registry status
Phase 3
Development phase
60 participants
Enrollment target
1
Study location

Study Summary

Study to provide initial data to assess the safety and efficacy of tegaserod use in patients with dyspepsia that are being treated with proton pump inhibitors (PPI's) for heartburn.

Conditions Studied

Interventions

  • DRUG Tegaserod

Study Locations (1)

New Jersey

  • http://www.novartisclinicaltrials.com/etrials/DiseaseID21/Dyspepsia-clinical-trials.go - East Hanover

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2005-04
Est. Completion 2006-08
Phase Phase 3
Novartis

265 total trials

What the finished NCT00171470 record still lists

NCT00171470 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 71-participant average among 11 other Dyspepsia trials with a reported enrollment target (15% lower).

The record links to 1 condition, with Dyspepsia appearing as the primary indexed condition, and to 1 intervention - of which Tegaserod is the first listed.

NCT00171470 reports a single indexed study location in New Jersey.

Frequently Asked Questions

What is clinical trial NCT00171470 about?

NCT00171470 is a clinical study titled "The Role of Tegaserod Therapy in the Management of Dyspeptic Symptoms in Female Patients on Proton Pump Inhibitors for the Treatment of Heartburn.". Study to provide initial data to assess the safety and efficacy of tegaserod use in patients with dyspepsia that are being treated with proton pump inhibitors (PPI's) for heartburn.

What is the current status of trial NCT00171470?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 60 participants. The study started on 2005-04. Estimated completion is 2006-08.

What conditions does trial NCT00171470 study?

This clinical trial studies the following conditions: Dyspepsia.

What interventions are being tested in trial NCT00171470?

The interventions under investigation include: Tegaserod (DRUG).

Who is sponsoring clinical trial NCT00171470?

This trial is sponsored by Novartis, which has 265 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00171470 being conducted?

This trial has 1 study location across New Jersey. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Dyspepsia

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00171470's enrollment target sits among peer trials

60 7th of 11 higher than 5 of 11 other Dyspepsia trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Dyspepsia trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00171470, the US trial registry maintained by the National Library of Medicine. NCT00171470 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.