Status:
COMPLETED
Obesity in HIV After Antiretroviral Therapy
Lead Sponsor:
Duke University
Collaborating Sponsors:
Janssen, LP
Conditions:
HIV
AIDS
Eligibility:
All Genders
18+ years
Brief Summary
This is a retrospective longitudinal study that evaluates the prevalence and incidence of overweight/obesity within an HIV-infected population before and after 12 and 24 months of a stable antiretrovi...
Eligibility Criteria
Inclusion
- Inclusion Criteria for HIV-infected cohort:
- Treatment-naive at study entry;
- Subjects will need to remain on ART for 12 months as initiated with substitution allowed for toxicity management within the same class of drug;
- Subjects within this group that remain on ART for an additional 12 months (total 24 months) as initiated with substitution allowed for toxicity management within the same class of drug will continue to be followed longitudinally for the 24 month period;
- Availability of repository samples.
- Inclusion Criteria for Control Cohort:
- Followed in the Duke Primary Care Clinics during the years of inclusion with available data on weight, race and gender.
Exclusion
- Exclusion Criteria for HIV-infected cohort:
- Pregnancy during period of observation or within 6 months of study entry;
- Malignancy (other than squamous or basal cell carcinomas of the skin);
- Newly diagnosed thyroid disorder within 6 months of study entry;
- Use of megace or marinol;
- Long-term use of glucocorticoids (greater than 1 month of prednisone 5mg or higher or an equivalent dose of another glucocorticoid);
- Use of androgenic steroids;
- History of diabetes or use of glucose-lowering agents;
- Use of the following psychiatric or anticonvulsant agents- thioridazine, olanzapine (zyprexa), clozapine (clozaril), quetiapine (seroquel), risperidone (risperdal), lithium, remeron, paxil, valproate, carbamazepine, gabapentin;
- Concurrent treatment for hepatitis C infection;
- Diagnosis of a new opportunistic infection (OI) as defined by the CDC during the 1st 12 months of ART.22 OIs include the following: PCP, toxoplasmosis, MAC, histoplasmosis, candidiasis, cryptococcus, coccidiodes, CMV, cryptosporidium, microsporidiosis, tuberculosis, bartonellosis, herpes simplex virus, HHV-8, human papillomavirus;
- Diagnosis of congestive heart failure and receiving diuretic therapy;
- End stage renal disease.
- Exclusion Criteria for Control Cohort:
- Pregnancy during period of observation or within 6 months of study entry;
- Malignancy (other than squamous or basal cell carcinomas of the skin);
- Newly diagnosed thyroid disorder within 6 months of study entry;
- Long-term use of glucocorticoids (greater than 1 month of prednisone 5mg or higher or an equivalent dose of another glucocorticoid);
- Use of androgenic steroids;
- History of diabetes or use of glucose-lowering agents;
- Use of the following psychiatric or anticonvulsant agents- thioridazine, olanzapine (zyprexa), clozapine (clozaril), quetiapine (seroquel), risperidone (risperdal), lithium, remeron, paxil, valproate, carbamazepine, gabapentin;
- Treatment for hepatitis C infection during observation period;
- Diagnosis of congestive heart failure and receiving diuretic therapy;
- End stage renal disease.
Key Trial Info
Start Date :
November 1 2009
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
May 1 2014
Estimated Enrollment :
200 Patients enrolled
Trial Details
Trial ID
NCT01461876
Start Date
November 1 2009
End Date
May 1 2014
Last Update
October 14 2015
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Duke University Medical Center
Durham, North Carolina, United States, 27710