NCT02240641

Brief Summary

The study aimed at comparing the evolution of renal function in patients showing a hypertension treated by various therapeutic strategies. Due to the contract research organisation (CRO) decision in September 2000, the database was locked and not accessible for Boehringer Ingelheim France. Consequently it was decided to stop the study and not proceed to the analysis. Thus, only safety data were processed in the safety database.

Trial Health

10
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
5,417

participants targeted

Target at P75+ for all trials

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 1998

Completed
2.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2000

Completed
14 years until next milestone

First Submitted

Initial submission to the registry

August 28, 2014

Completed
19 days until next milestone

First Posted

Study publicly available on registry

September 16, 2014

Completed
Last Updated

September 16, 2014

Status Verified

September 1, 2014

Enrollment Period

2.3 years

First QC Date

August 28, 2014

Last Update Submit

September 15, 2014

Conditions

Outcome Measures

Primary Outcomes (1)

  • Number of patients with adverse events

    up to two years

Study Arms (1)

hypertension treatment strategies

Drug: LacidipineDrug: DiureticsDrug: antihypertensive drugsDrug: alpha blockersDrug: Angiotensin-Converting Enzyme InhibitorsDrug: beta blockers

Interventions

Also known as: Caldine
hypertension treatment strategies
hypertension treatment strategies
hypertension treatment strategies
hypertension treatment strategies
hypertension treatment strategies
hypertension treatment strategies

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

patients with hypertension requiring treatment

You may qualify if:

  • patients with hypertension requiring treatment

You may not qualify if:

  • none

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Hypertension

Interventions

lacidipineDiureticsAntihypertensive AgentsAdrenergic alpha-AntagonistsAngiotensin-Converting Enzyme InhibitorsAdrenergic beta-Antagonists

Condition Hierarchy (Ancestors)

Vascular DiseasesCardiovascular Diseases

Intervention Hierarchy (Ancestors)

Natriuretic AgentsPhysiological Effects of DrugsPharmacologic ActionsChemical Actions and UsesCardiovascular AgentsTherapeutic UsesAdrenergic AntagonistsAdrenergic AgentsNeurotransmitter AgentsMolecular Mechanisms of Pharmacological ActionProtease InhibitorsEnzyme Inhibitors

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 28, 2014

First Posted

September 16, 2014

Study Start

May 1, 1998

Primary Completion

September 1, 2000

Last Updated

September 16, 2014

Record last verified: 2014-09