CClinicalTrials.gg
Status unknownNCT00251849Updated Aug 21, 2008

PROVIDENCE-1: Study of Rifalazil in Chlamydia Pneumoniae Seropositive Patients

A Phase 3 interventional study of Rifalazil in Peripheral Vascular Diseases and Intermittent Claudication, sponsored by ActivBiotics. Status unknown at 48 sites in 3 countries. Open to participants aged 40 Years to 80 Years. Per ClinicalTrials.gov, last updated 2008-08-21.

Sponsored by ActivBiotics · Phase 3, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Oct 2006), so the status shown — last known as Active, not recruiting — may be out of date.
Phase
Phase 3
Study type
Interventional
Enrollment
274
Allocation
Randomized
Ages
40 Years to 80 Years
Sex
All
01

Study summary

The objective of this study is to determine whether rifalazil can significantly increase peak walking time (PWT) in patients with peripheral arterial disease (PAD).

02

Conditions studied

  • Peripheral Vascular Diseases
  • Intermittent Claudication

Keywords

  • Intermittent Claudication
03

In context

Vascular Diseases

1,027 studies on the registry are indexed under Vascular Diseases; 167 are open to participants now.

This study's enrollment of 274 is above the median of 78 across 639 interventional studies indexed under Vascular Diseases.

Browse Vascular Diseases studies →

Lead sponsor

This is the only study on the registry with ActivBiotics as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Male or female patients between 40 and 80 years of age, inclusive.
  • The patient has seropositive evidence of Chlamydia pneumoniae defined by immunoglobulin G antibody titers.
  • The patient has a diagnosis of intermittent claudication due to PAD at screening.
  • The patient's maximal effort PWT is limited only by severe claudication symptoms.
  • If the patient is taking cilostazol or pentoxifylline and has been on a stable dose of the medication for at least 6 months prior to screening. Patients who have recently discontinued medications for PAD and/or intermittent claudication must "wash-out" for at least one month prior to screening.
  • The patient has been on a stable dose of statin therapy for at least 6 months prior to screening.Patients who have recently discontinued statin therapy must "wash-out" for at least one month prior to screening.
  • Male and female patients must agree to use an effective form of birth control throughout the study period.

Exclusion criteria

Exclusion Criteria:

  • The patient has critical limb ischemia as evidenced by ischemic rest pain, ulceration, or gangrene.
  • The patient has had a major amputation of the leg or any other amputation that limits walking ability.
  • The patient is planned for surgical/endovascular intervention for PAD during the course of the study.
  • The patient has or is being treated or evaluated for tuberculosis.
  • The patient has a known immunodeficient state (e.g., positive for human immunodeficiency virus) or is being treated with immunosuppressive drugs including high dose steroids or cyclosporine.
  • The patient has an active infection requiring systemic or oral antibiotics.
  • The patient has an uncontrolled, unstable or recently diagnosed autoimmune disease, including but not limited to systemic lupus, inflammatory bowel disease, sarcoidosis, rheumatoid arthritis, or psoriasis. Patients who develop autoimmune disease during the course of the study must be withdrawn.
  • The patient's PWT is limited by symptoms other than claudication (shortness of breath, fatigue, angina, or arthritis).
  • The patient has a history of alcohol abuse, illicit drug use or drug abuse or significant mental illness.
  • The patient has a known or suspected allergy to the study medication(s) or class of study medication (rifamycins) to be administered.
  • The patient chronically uses antibacterials or has previously received rifalazil or any rifamycin (e.g. rifampin).
  • The patient has uncontrolled hypertension (resting blood pressure > 160/100 mm Hg), uncontrolled moderate to severe congestive heart failure (CHF), or uncontrolled arrhythmic disorders.
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double
Enrollment
274 participants

Interventions

  • DrugRifalazil
06

What researchers measure

Primary outcomes

  1. The efficacy endpoint is change from baseline in PWT

  2. The safety endpoints are adverse event rates, rates of clinically significant laboratory abnormalities, vital signs, and physical exam abnormalities, rate of vascular death, myocardial infarction (MI), stroke, revascularization or vascular procedures

07

Study locations

48 sites
  • Scottsdale Cardiovascular Research Institute
    Scottsdale, Arizona 85251, United States
  • VA Palo Alto Health Care System
    Palo Alto, California 94304, United States
  • Siddeg, Inc.
    San Diego, California 92103, United States
  • Apex Research Institute
    Santa Ana, California 92705, United States
  • Radiant Research
    Santa Rosa, California 95405, United States
  • Aurora Denver Cardiology Associates
    Denver, Colorado 80218, United States
  • Tampa Bay Medical Research, Inc.
    Clearwater, Florida 33761, United States
  • Jacksonville Center for Clinical Research
    Jacksonville, Florida 32216, United States
  • University Clinical Research
    Pembrook Pines, Florida 33024, United States
  • Cardiovascular Center of Sarasota
    Sarasota, Florida 34239, United States
  • Rockdale Medical Research Associates
    Conyers, Georgia 30094, United States
  • The Care Group
    Indianapolis, Indiana 46290, United States
  • Androscoggin Cardiology Associates
    Auburn, Maine 04210, United States
  • University of Massachusetts Medical Center
    Worcester, Massachusetts 01655, United States
  • St. Louis University
    St. Louis, Missouri 63104, United States
  • Durham VA Medical Center
    Durham, North Carolina 27705, United States
  • New Hope Research of Oregon, Inc.
    Portland, Oregon 97219, United States
  • Radiant Research
    Philadelphia, Pennsylvania 19115, United States
  • Omega Medical Research
    Warwick, Rhode Island 02886, United States
  • Black Hills Clinical Research Center
    Rapid City, South Dakota 57701, United States
  • Hampton Roads Center for Clinical Research
    Norfolk, Virginia 23502, United States
  • National Clinical Research
    Richmond, Virginia 23294, United States
  • Care Foundation
    Wausau, Wisconsin 54401, United States
  • Hospital e Maternidade Dr. Christovao da Gama
    Santo Andre, SP 09030-010, Brazil
  • Centro de Ciencias Medicas e Biologicas da Pontificia Universidade
    Sorocaba, SP 18031-000, Brazil
  • Depto de Cirurgia e ortopedia
    Botucatu, 18618-970, Brazil
  • SMHS - Area Especial
    Brasilia, 70330-150, Brazil
  • Hospital Pedro Ernesto
    Rio de Janeiro, Brazil
  • Instituto de molestias cardiovasculares
    Sao Jose do Rio Preto, 15015-210, Brazil
  • Vishnevsky Institute of Surgery
    Moscow, 113093, Russian Federation
  • Russian State Medical University
    Moscow, 115516, Russian Federation
  • Russian State Medical University
    Moscow, 117049, Russian Federation
  • Central Clinical Hospital #1
    Moscow, 125367, Russian Federation
  • City Hospital # 13
    Nizhniy Novgorod, 603018, Russian Federation
  • Meshalkin Research Institute of Blood Circulation Pathology
    Novosibirsk, 630055, Russian Federation
  • Saint Petersburg Djanelidze Research Institute of First Aid
    Saint Petersburg, 192242, Russian Federation
  • Saint Petersburg State Medical Pediatric Academy
    Saint Petersburg, 194100, Russian Federation
  • Research Institute of Cardiology n.a. Almazov
    Saint Petersburg, 194156, Russian Federation
  • City Hospital #26
    Saint Petersburg, 196247, Russian Federation
  • Saint Petersburg Pavlov Medical University
    Saint Petersburg, 197022, Russian Federation
  • City Hospital #2
    Saint-Petersburg, 194354, Russian Federation
  • Pokrovskaya Hospital
    Saint-Petersburg, 199106, Russian Federation
  • City Clinical Hospital # 1
    Saratov, 410017, Russian Federation
  • Clinical Hospital #1
    Smolensk, 214000, Russian Federation
  • Dzhanelidze Emergency Medicine Research Institutes
    St. Petersburg, 192242, Russian Federation
  • Tomsk Research Center
    Tomsk, 643012, Russian Federation
  • Regional Clinical Hospital
    Vladimir, 600023, Russian Federation
  • Clinical City Hospital # 25
    Volgograd, 400138, Russian Federation
08

References and documents

Publications

  • Jaff MR, Dale RA, Creager MA, Lipicky RJ, Constant J, Campbell LA, Hiatt WR. Anti-chlamydial antibiotic therapy for symptom improvement in peripheral artery disease: prospective evaluation of rifalazil effect on vascular symptoms of intermittent claudication and other endpoints in Chlamydia pneumoniae seropositive patients (PROVIDENCE-1). Circulation. 2009 Jan 27;119(3):452-8. doi: 10.1161/CIRCULATIONAHA.108.815308. Epub 2009 Jan 12. PubMed 19139383 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 21, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00251849
Lead sponsor
ActivBiotics
First posted
Nov 11, 2005
Start date
Nov 2005
Completion
Dec 2007
Last update
Aug 21, 2008
View the source record on ClinicalTrials.gov ↗

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