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NCT01939496 · ClinicalTrials.gov registry record · Phase 4

Evaluation of Blood Pressure Reduction, Safety, and Tolerability of Canagliflozin in Patients With Hypertension and Type 2 Diabetes Mellitus on Stable Doses of Anti-hyperglycemic and Anti-hypertensive Agents

A Phase 4 study, sponsored by Janssen Scientific Affairs.

Completed
Registry status
Phase 4
Development phase
171
Enrollment target

NCT01939496: Completed Phase 4 study, sponsored by Janssen Scientific Affairs.

NCT01939496 is a Phase 4 study that has completed, run by Janssen Scientific Affairs. The registered enrollment target is 171 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01939496, a Phase 4 study, has completed, sponsored by Janssen Scientific Affairs.

COMPLETED
Registry status
Phase 4
Development phase
171 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the effect of canagliflozin (JNJ-28431754) on blood pressure reduction, compared to placebo, in patients with hypertension and type 2 diabetes mellitus and who are on stable doses of anti-hyperglycemic and anti-hypertensive agents. Overall safety and tolerability of canagliflozin will be assessed.

Primary Outcome

The blood pressure (BP) was evaluated by Ambulatory Blood Pressure Monitoring (ABPM) for all participants based on the 24-hour BP recordings.

Interventions

  • DRUG Placebo
  • DRUG Canagliflozin

Trial Details

FieldValue
Enrollment Target 171 participants
Start Date 2013-10
Est. Completion 2015-04
Phase Phase 4
Janssen Scientific Affairs

37 total trials

What the finished NCT01939496 record still lists

NCT01939496 is an interventional study that assigns participants to a tested intervention. The registered 171 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (67% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT01939496 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01939496 about?

NCT01939496 is a clinical study titled "Evaluation of Blood Pressure Reduction, Safety, and Tolerability of Canagliflozin in Patients With Hypertension and Type 2 Diabetes Mellitus on Stable Doses of Anti-hyperglycemic and Anti-hypertensive Agents". The purpose of this study is to evaluate the effect of canagliflozin (JNJ-28431754) on blood pressure reduction, compared to placebo, in patients with hypertension and type 2 diabetes mellitus and who are on stable doses of anti-hyperglycemic and anti-hypertensive agents. Overall safety and tolerabi...

What is the current status of trial NCT01939496?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 171 participants. The study started on 2013-10. Estimated completion is 2015-04.

What interventions are being tested in trial NCT01939496?

The interventions under investigation include: Placebo (DRUG), Canagliflozin (DRUG).

Who is sponsoring clinical trial NCT01939496?

This trial is sponsored by Janssen Scientific Affairs, which has 37 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01939496's enrollment target sits among peer trials

171 484th of 2000 higher than 1,517 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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 NCT01939496, the US trial registry maintained by the National Library of Medicine. NCT01939496 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.