Skip to content

Study “before-after”: Adherence Evaluation to antiretroviral therapy administered in two different ways

Study “before-after”: Adherence Evaluation to antiretroviral therapy administered in two different ways: - EPIVIR (3TC) + VIREAD (TDF) versus TRUVADA (FTC + TDF) - EPIVIR (3TC) + ZIAGEN (ABC) versus KIVEXA (3TC + ABC) - EPIVIR (3TC) + RETROVIR (AZT) versus COMBIVIR (3TC + AZT) - EPIVIR (3TC) + VIREAD (TDF) + EFAVIRENZ (EFV) versus ATRIPLA (3TC + TDF + EFV)

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2011-004935-30-IT
Enrollment
Unknown
Registered
2012-03-08
Start date
2011-11-22
Completion date
Unknown
Last updated
2012-10-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV infection MedDRA version: 14.1 Level: PT Classification code 10020161 Term: HIV infection System Organ Class: 10021881 - Infections and infestations

Interventions

Trade Name: EPIVIR*FL 30CPR RIV 300MG Pharmaceutical Form: Film-coated tablet INN or Proposed INN: LAMIVUDINE CAS Number: 134678-17-4 Current Sponsor code: NA Other descriptive name: NA Concentration

Sponsors

U.L.S.S. 9 DI TREVISO
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - age: at least 18 years old or older - patient treated with Truvada or Kivexa or Combivir and 3th drugs or Atripla for at least 6 months - Viral load =65 years) no F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: patients who are at risk of non adherence (alcoholic abuse, intravenous drug users, dementia, language difficulties, homeless).

Design outcomes

Primary

MeasureTime frame
Secondary Objective: To compare the adherence in the two groups receiving the same HAART with different kind of administration (co-formulated versus multiple pills).;Primary end point(s): Evaluation of the adherence difference between baseline and 4-6 months afterwards in the two groups, one switched from co-formulated therapy to more pills, and one continuing co-formulated therapy.;Timepoint(s) of evaluation of this end point: 4-6 months;Main Objective: To compare the adherence in the group switching from co-formulated drugs to multiple pills.

Secondary

MeasureTime frame
Secondary end point(s): NA;Timepoint(s) of evaluation of this end point: NA

Countries

Italy

Contacts

Public ContactNUCLEO DI RICERCA CLINICA

ULSS n. 9 di TREVISO

segcomitatoeticotv@ulss.tv.it0422 32 8268

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026