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A Study on Antiretroviral Therapy (ART) Naïve Patients On Different Regimens to Treat Hiv (NORTHIV)

This study has been completed.
Information provided by (Responsible Party):
Lars-Magnus Andersson, Göteborg University Identifier:
First received: September 28, 2011
Last updated: October 2, 2011
Last verified: October 2011
The present study aims to compare efficacy, side-effects, and treatment adherence of three different treatment regimens given to antiretroviral naïve HIV-1 infected patients. Treatment will be initiated in accordance with the Swedish National Guidelines. In the twice daily (BID) arm (1), which could be considered as a standard regimen at present, lopinavir/ritonavir, is co-administrated with 2 nucleoside reverse transcriptase inhibitors (NRTIs) administrated BID. The first once daily (QD) arm (2) combines the protease inhibitor (PI) atazanavir/ritonavir with 2 NRTIs administrated QD, and in the second QD arm (3), the non nucleoside reverse transcriptase inhibitor (NNRTI) efavirenz is combined with 2 NRTIs administrated QD. All drugs used in the study are licensed in the participating countries and patients will be followed as in clinical practice. Patients could optionally, after informed consent, be followed with additional measurements of HIV-1 RNA after 1, 2, and 3 weeks of treatment to asses the kinetics of viral decline after initiation of treatment.

Condition Intervention Phase
Drug: Lopinavir ritonavir
Drug: Atazanavir ritonavir
Drug: Efavirenz
Phase 4

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: A Study on ART Naïve Patients On Different Regimens to Treat Hiv (a Phase 4 Study)

Resource links provided by NLM:

Further study details as provided by Göteborg University:

Primary Outcome Measures:
  • Intention to treat (ITT)/time to loss of virological response (TLOVR) [ Time Frame: 144 weeks ]
    1. Virological failure (see 5.5.2 for definition)
    2. Treatment interruption or change of study treatment due to side-effects
    3. Treatment interruption or change of study treatment due to any other reason
    4. Missed to follow-up

    1. HIV-1 RNA >50 copies/ml in two consecutive measurements from week 24 and on 2. any rise in HIV-1 RNA >50 copies/ml in two consecutive measurements after viral load <50 copies/ml has been reached 3. HIV-1 RNA never <50 copies/ml after week 24

Secondary Outcome Measures:
  • Frequency of abnormal laboratory parameters [ Time Frame: 144 weeks ]
    Incidence of abnormal laboratory parameters at follow-up

  • Adherence to study medication [ Time Frame: 144 weeks ]
    Proportion of doses taken correctly

  • Frequency of adverse events [ Time Frame: 144 weeks ]
    Proportion of treatment discontinuations and changes due to different adverse events

  • Changes in CD4 cell counts [ Time Frame: 144 weeks ]
    Changes in CD4+ T-cell count from baseline

  • Changes in plasma lipids [ Time Frame: 144 weeks ]
    Changes from baseline in plasma lipids

  • Frequency of hyperlipidemia [ Time Frame: 144 weeks ]
    Incidence of hypercholesterolemia and hypertriglyceridemia at baseline and follow-up

Enrollment: 242
Study Start Date: April 2004
Study Completion Date: December 2009
Primary Completion Date: December 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: lopinavir/ritonavir
400/100 mg BID + 2 NRTIs BID
Drug: Lopinavir ritonavir
400mg BD 100mg BD
Active Comparator: atazanavir/ritonavir
300mg+100mg QD+ 2 NRTI QD
Drug: Atazanavir ritonavir
300mg QD 100mg QD
Active Comparator: efavirenz
600mg QD + 2NRTI QD
Drug: Efavirenz
600mg QD


Ages Eligible for Study:   16 Years and older   (Child, Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Male or female, aged 16 years of age
  • HIV-1 infected as documented by a licensed HIV-1 antibody ELISA
  • Ability to understand and provide informed consent
  • Indication for antiretroviral treatment
  • Antiretroviral naïve
  • All clinical laboratory values not clinically significant

Exclusion Criteria:

  • Subjects being pregnant
  • Women of childbearing potential not practicing birth control
  • Subjects with renal failure requiring dialysis
  • Drug interactions with any of the study drugs that are not manageable
  • Resistance to any of the study drugs
  Contacts and Locations
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Please refer to this study by its identifier: NCT01445223

Department of Infectious Diseases
Goteborg, Sweden, S-41685
Sponsors and Collaborators
Göteborg University
Principal Investigator: Magnus Gisslén, Professor Goteborg Universitet
  More Information

Additional Information:
Publications automatically indexed to this study by Identifier (NCT Number):
Responsible Party: Lars-Magnus Andersson, Principal Investigator, Göteborg University Identifier: NCT01445223     History of Changes
Other Study ID Numbers: Northiv protocol 3.66
Study First Received: September 28, 2011
Last Updated: October 2, 2011

Keywords provided by Göteborg University:
Antiretroviral therapy
randomised controlled clinical trial

Additional relevant MeSH terms:
Atazanavir Sulfate
HIV Protease Inhibitors
Protease Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Anti-HIV Agents
Anti-Retroviral Agents
Antiviral Agents
Anti-Infective Agents
Cytochrome P-450 CYP3A Inhibitors
Cytochrome P-450 Enzyme Inhibitors
Reverse Transcriptase Inhibitors
Nucleic Acid Synthesis Inhibitors
Cytochrome P-450 CYP2C9 Inhibitors
Cytochrome P-450 CYP2C19 Inhibitors
Cytochrome P-450 CYP2B6 Inducers
Cytochrome P-450 Enzyme Inducers
Cytochrome P-450 CYP3A Inducers processed this record on April 24, 2017