Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional

Six Month Clinical Trial Assessing Efficacy and Safety of Inhaled Insulin in Type 1 Diabetes

ClinicalTrials.gov ID: NCT00424333

Public ClinicalTrials.gov record NCT00424333. 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 30, 2026, 4:28 PM EDT

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

Official title

Efficacy and Safety of Inhaled Compared With Subcutaneous Human Insulin in an Intensive Insulin Regimen for Subjects With Type 1 Diabetes Mellitus: A Six-Month, Outpatient, Parallel Comparative Trial

Brief summary

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

To determine in subjects with Type 1 Diabetes Mellitus: 1. Whether glycemic control can be achieved at least as effectively with a) an intensive insulin regimen involving pre-meal inhaled insulin plus twice daily subcutaneous NPH insulin as with b) an intensive subcutaneous insulin regimen involving pre-meal regular insulin plus twice daily NPH, given as 4 injections per day. The treatment regimens differ only by the route of delivery of the short acting insulin. 2. The toleration and safety of inhaled insulin therapy and its effects after 6months, if any, on measures of pulmonary function.

Study identification

NCT ID
NCT00424333
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
320 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
12 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
May 1999 (Type not available)
Primary completion
Not listed
Completion
Oct 2000 (Type not available)
Last update posted
Feb 13, 2007

1999 – 2000

United States locations

U.S. sites
30
U.S. states
17
U.S. cities
30
Facility City State ZIP Site status
Pfizer Investigational Site Duarte California — —
Pfizer Investigational Site Long Beach California — —
Pfizer Investigational Site Los Angeles California — —
Pfizer Investigational Site Stanford California — —
Pfizer Investigational Site Denver Colorado — —
Pfizer Investigational Site New Haven Connecticut — —
Pfizer Investigational Site Gainesville Florida — —
Pfizer Investigational Site Hollywood Florida — —
Pfizer Investigational Site Miami Florida — —
Pfizer Investigational Site Tallahassee Florida — —
Pfizer Investigational Site Peoria Illinois — —
Pfizer Investigational Site Skokie Illinois — —
Pfizer Investigational Site Lutherville Maryland — —
Pfizer Investigational Site Waltham Massachusetts — —
Pfizer Investigational Site Minneapolis Minnesota — —
Pfizer Investigational Site Columbia Missouri — —
Pfizer Investigational Site New Hyde Park New York — —
Pfizer Investigational Site Rochester New York — —
Pfizer Investigational Site Syracuse New York — —
Pfizer Investigational Site The Bronx New York — —
Pfizer Investigational Site Durham North Carolina — —
Pfizer Investigational Site Winston-Salem North Carolina — —
Pfizer Investigational Site Portland Oregon — —
Pfizer Investigational Site Pittsburgh Pennsylvania — —
Pfizer Investigational Site Dallas Texas — —
Pfizer Investigational Site Houston Texas — —
Pfizer Investigational Site Burlington Vermont — —
Pfizer Investigational Site Charlottesville Virginia — —
Pfizer Investigational Site Charlottsville Virginia — —
Pfizer Investigational Site Seattle Washington — —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00424333, 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 Feb 13, 2007 · Synced Oct 30, 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 NCT00424333 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →