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Omega-3 Supplementation in HIV Patients With Therapeutic Lifestyle Change Diet.

Primary Purpose

Human Immunodeficiency Virus

Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Omega-3 fatty acids
TLC nutritional intervention
Omega-3 fatty acid supplementation with fish oil and TLC nutritional intervention.
Sponsored by
Instituto Mexicano del Seguro Social
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Human Immunodeficiency Virus focused on measuring Omega-3 Fatty Acids, Therapeutic Lifestyle Changes, Human Immunodeficiency Virus, Cardiac Risk, Dyslipidemia

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients positive to Human Immunodeficiency Virus or Acquired Immunodeficiency Syndrome
  • Patients older than 18 years positive to HIV/AIDS with HAART
  • Patients who agreed to sign consent under written information
  • Patients that had some type of dyslipidemia according the Mexican Norms of 2002.

Exclusion Criteria:

  • Patient with mouth non-permeable
  • Patients with intolerance or allergy to fish oil
  • Patient record in the database SMART but inactive.
  • Patients who use or have used in the last 6 weeks food supplements that modify lipids.
  • Patient who have not attended two of the four set appointments for valuation.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm 4

    Arm 5

    Arm Type

    Experimental

    Active Comparator

    Experimental

    Active Comparator

    Placebo Comparator

    Arm Label

    Group one

    Group two

    Group three

    Group four

    Group five

    Arm Description

    20 subjects received Therapeutic Lifestyle Changes diet more 1.05 grams of fish oil omega 3 fatty acids

    20 subjects received conventional diet more 1.05 grams of fish oil omega 3 fatty acids

    20 subjects received Therapeutic Lifestyle Changes diet more 2.10 grams of fish oil omega 3 fatty acids.

    20 subjects received conventional diet more 2.10 grams of fish oil omega 3 fatty acids

    20 subjects, control group received conventional diet.

    Outcomes

    Primary Outcome Measures

    Triglycerides (TG)
    Serum TG measured at baseline, before initiating treatment.
    Total cholesterol (TC)
    Serum TC measured at baseline, before initiating treatment.
    High density cholesterol (HD-C)
    Serum HD-C measured at baseline, before initiating treatment
    Low density cholesterol (LD-C)
    Serum LD-C measured at baseline, before initiating treatment
    Very low density cholesterol (VLD-C)
    Serum VLD-C measured at baseline, before initiating treatment
    Body weight
    Total weight before initiating treatment.
    Body mass index (BMI)
    BMI obtained before initiating treatment
    TG 4
    Serum TG measured at week four of treatment.
    TC 4
    Serum TC measured at week four of treatment.
    HD-C 4
    Serum HD-C measured at week four of treatment.
    LD-C 4
    Serum LD-C measured at week four of treatment.
    VLD-C 4
    Serum VLD-C measured at week four of treatment.
    Weight 4
    Total weight before at week four of treatment.
    BMI 4
    BMI obtained at week four of treatment
    TG 12
    Serum TG measured at week four of treatment.
    TC 12
    Total serum TG measured at week twelve of treatment
    HD-C 12
    Serum HD-C measured at week twelve of treatment
    LD-C 12
    Serum LD-C measured at week twelve of treatment
    VLD-C 12
    Serum VLD-C measured at week twelve of treatment
    Weight 12
    Total weight before at week twelve of treatment.
    BMI 12
    BMI obtained at week twelve of treatment

    Secondary Outcome Measures

    Full Information

    First Posted
    August 28, 2015
    Last Updated
    September 1, 2015
    Sponsor
    Instituto Mexicano del Seguro Social
    Collaborators
    Hospital Civil de Guadalajara
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02537236
    Brief Title
    Omega-3 Supplementation in HIV Patients With Therapeutic Lifestyle Change Diet.
    Official Title
    Efficacy and Safety of Fish Oil (Omega-3 Fatty Acid) Supplementation With Therapeutic Lifestyle Changes Diet Associated With Lipidic Profile in HIV-positive Patients With Antiretroviral Therapy.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2015
    Overall Recruitment Status
    Completed
    Study Start Date
    January 2009 (undefined)
    Primary Completion Date
    May 2009 (Actual)
    Study Completion Date
    December 2009 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Instituto Mexicano del Seguro Social
    Collaborators
    Hospital Civil de Guadalajara

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The positive patients to the Human Immunodeficiency Virus (HIV) with Highly Active Antiretroviral Therapy (HAART) present multiple alterations in their corporal composition and dyslipidemia, wich increase the cardiovascular risk. The investigators evaluated the efficiency of the combination of fish oil omega 3 fatty acids to different doses with the Therapeutic Lifestyle Changes (TLC) diet of the National Cholesterol Education Program on the profile of lipids and the corporal weight in patients with HIV treated with HAART.
    Detailed Description
    The infection by Human Immunodeficiency Virus (HIV) or Acquired Immunodeficiency Syndrome (AIDS), is a chronic condition transmissible and progressive type of viral cause, in which a link is very different between host and virus, which ultimately influences the appearance of opportunistic morbid processes or rare tumors, or both1. With a prevalence of 3 cases for every 1000 people from 15 to 49 years, Mexico ranks 16th place in the prevalence of HIV/AIDS in adults in Latin America2. The state of Jalisco, México, occupies the fourth place in terms of positive cases of HIV-AIDS, in this same plane, the municipalities of Guadalajara, Zapopan, Tlaquepaque and Puerto Vallarta in Jalisco, represent the main populations with the highest number of positive cases by HIV-AIDS. The HIV positive individuals with Highly Active Antiretroviral Therapy (HAART) or without treatment are facing numerous challenges in terms of management of their health; some of the most disturbing changes are visible in the shape and appearance of the body. In most cases this anatomical changes come accompanied by alterations in biochemical indicators: lipid levels (cholesterol and triglycerides) and insulin resistance4.These adverse effects may have important clinical implications, such as severe lactic acidosis, coronary artery disease and acute pancreatitis5. In patients with HIV and HAART has published an incidence of hypercholesterolemia and hypertriglyceridemia between 5 and 90% depending on the series, although the true incidence is yet to be determined6. Pharmacological interventions with statins or fibrates in patients infected with HIV are limited partially due to the drug interactions and increase in the frequency of adverse effects7. Therefore, it is necessary to investigate new alternatives for the management of dyslipidemia in patients infected with HIV with HAART through changes in diet and supplements of fish oil omega 3 fatty acids. Methods Patients: The investigators enrolled 100 Patients positive to Human Immunodeficiency Virus or Acquired Immunodeficiency Syndrome, and had been receiving ≥2 Highly Active Antiretroviral Therapy, and with diagnostic of dislipidemia according the Mexican Official Standard Norms of 2002, for the prevention, treatment and control of dyslipidemias8. All the patients were active in the SMART database from HIV/AIDS department of the Civil Hospital in Guadalajara "Fray Antonio Alcalde". Patients were excluded for intolerance or allergy to fish, patients that use or have used in the last 6 weeks supplements or drugs that modify lipids. Study design During the period from January 2010 to July 2011, was carried out the study with the authorization of the ethics committee of the Civil Hospital in Guadalajara "Fray Antonio Alcalde". Our subjects were assigned to 5 intervention groups: Groups one= 20 subjects received Therapeutic Lifestyle Changes diet more 1.05 grams of Fatty Acid omega 3. Groups two= 20 subjects received conventional diet more 1.05 grams of Fatty Acid omega three. Groups 3=20 subjects received Therapeutic Lifestyle Changes diet more 2.10 grams of Fatty Acid omega 3. Groups four=20 subjects received conventional diet more 2.10 grams of Fatty Acid omega 3. Groups five= 20 subjects, control group received conventional diet. The subject assigned to group one and three with TLC diet, received advice from the nutritionist in week 4 and 12 to encourage the consumption of the capsules of omega 3 fatty acids, in addition offered general recommendations to consume dietary fiber and fluids. The subject assigned to groups two and four with conventional diet, received advice from the nutritionist in the week 4 and 12 to encourage the consumption of the capsules of omega 3 fatty acids without the assistance of special diet. The requirements of energy and macronutrients were identified in the patients of group one and three. None of the subjects received advice on the physical activity that could perform. Statistical analysis The main objective of this study was to compare the changes in fasting levels of triglycerides (TG), total cholesterol (TC), high density cholesterol (HD-C), low density cholesterol (LD-C), very low density cholesterol (VLD-C), the body weight and body mass index (BMI) against the week 4 and 12. The safety and tolerability of the study medication were also secondary outcomes. Statistical analysis was carried out starting with the Kolmogorov-Smirnov test to identify the distribution of variables, then identify the type of distribution of each variable, is continuous with the descriptive statistical analysis for variables with abnormal distribution -non-parametric, with measures of central tendency and dispersion as: the median distance and interquartiles and variables with normal distribution - parametric- :the mean and standard deviation. Inferential analysis to the intra-group used the Wilcoxon test and Friedman. For the inferential analysis between groups was implemented in the variables of non-normal distribution, the Kruskal-Wallis test; and for variables with normal distribution was used the one-way ANOVA test. Differences were considered statistically significant when the p value was <0.05 . The data were processed using the statistical package No.18.0 and are presented in tables and graphics.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Human Immunodeficiency Virus
    Keywords
    Omega-3 Fatty Acids, Therapeutic Lifestyle Changes, Human Immunodeficiency Virus, Cardiac Risk, Dyslipidemia

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderInvestigator
    Allocation
    Randomized
    Enrollment
    200 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Group one
    Arm Type
    Experimental
    Arm Description
    20 subjects received Therapeutic Lifestyle Changes diet more 1.05 grams of fish oil omega 3 fatty acids
    Arm Title
    Group two
    Arm Type
    Active Comparator
    Arm Description
    20 subjects received conventional diet more 1.05 grams of fish oil omega 3 fatty acids
    Arm Title
    Group three
    Arm Type
    Experimental
    Arm Description
    20 subjects received Therapeutic Lifestyle Changes diet more 2.10 grams of fish oil omega 3 fatty acids.
    Arm Title
    Group four
    Arm Type
    Active Comparator
    Arm Description
    20 subjects received conventional diet more 2.10 grams of fish oil omega 3 fatty acids
    Arm Title
    Group five
    Arm Type
    Placebo Comparator
    Arm Description
    20 subjects, control group received conventional diet.
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    Omega-3 fatty acids
    Other Intervention Name(s)
    eicosapentaenoic acid, docosahexaenoic acid
    Intervention Description
    Omega-3 fatty acid supplementation with fish oil.
    Intervention Type
    Behavioral
    Intervention Name(s)
    TLC nutritional intervention
    Intervention Description
    nutritional orientation.
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    Omega-3 fatty acid supplementation with fish oil and TLC nutritional intervention.
    Intervention Description
    Omega 3 fatty acid supplementation with fish oil and nutritional counseling of TLC diet.
    Primary Outcome Measure Information:
    Title
    Triglycerides (TG)
    Description
    Serum TG measured at baseline, before initiating treatment.
    Time Frame
    At baseline
    Title
    Total cholesterol (TC)
    Description
    Serum TC measured at baseline, before initiating treatment.
    Time Frame
    At baseline
    Title
    High density cholesterol (HD-C)
    Description
    Serum HD-C measured at baseline, before initiating treatment
    Time Frame
    At baseline
    Title
    Low density cholesterol (LD-C)
    Description
    Serum LD-C measured at baseline, before initiating treatment
    Time Frame
    At baseline
    Title
    Very low density cholesterol (VLD-C)
    Description
    Serum VLD-C measured at baseline, before initiating treatment
    Time Frame
    At baseline
    Title
    Body weight
    Description
    Total weight before initiating treatment.
    Time Frame
    At baseline
    Title
    Body mass index (BMI)
    Description
    BMI obtained before initiating treatment
    Time Frame
    At baseline
    Title
    TG 4
    Description
    Serum TG measured at week four of treatment.
    Time Frame
    At week four of treatment
    Title
    TC 4
    Description
    Serum TC measured at week four of treatment.
    Time Frame
    At week four of treatment
    Title
    HD-C 4
    Description
    Serum HD-C measured at week four of treatment.
    Time Frame
    At week four of treatment
    Title
    LD-C 4
    Description
    Serum LD-C measured at week four of treatment.
    Time Frame
    At week four of treatment
    Title
    VLD-C 4
    Description
    Serum VLD-C measured at week four of treatment.
    Time Frame
    At week four of treatment
    Title
    Weight 4
    Description
    Total weight before at week four of treatment.
    Time Frame
    At week four of treatment
    Title
    BMI 4
    Description
    BMI obtained at week four of treatment
    Time Frame
    At week four of treatment
    Title
    TG 12
    Description
    Serum TG measured at week four of treatment.
    Time Frame
    At week twelve of treatment
    Title
    TC 12
    Description
    Total serum TG measured at week twelve of treatment
    Time Frame
    At week twelve of treatment
    Title
    HD-C 12
    Description
    Serum HD-C measured at week twelve of treatment
    Time Frame
    At week twelve of treatment
    Title
    LD-C 12
    Description
    Serum LD-C measured at week twelve of treatment
    Time Frame
    At week twelve of treatment
    Title
    VLD-C 12
    Description
    Serum VLD-C measured at week twelve of treatment
    Time Frame
    At week twelve of treatment
    Title
    Weight 12
    Description
    Total weight before at week twelve of treatment.
    Time Frame
    At week twelve of treatment
    Title
    BMI 12
    Description
    BMI obtained at week twelve of treatment
    Time Frame
    At week twelve of treatment

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    60 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients positive to Human Immunodeficiency Virus or Acquired Immunodeficiency Syndrome Patients older than 18 years positive to HIV/AIDS with HAART Patients who agreed to sign consent under written information Patients that had some type of dyslipidemia according the Mexican Norms of 2002. Exclusion Criteria: Patient with mouth non-permeable Patients with intolerance or allergy to fish oil Patient record in the database SMART but inactive. Patients who use or have used in the last 6 weeks food supplements that modify lipids. Patient who have not attended two of the four set appointments for valuation.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Alejandro González-Ojeda, MD. PhD. F.A.C.S.
    Organizational Affiliation
    Instituto Mexicano del Seguro Social
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    9619798
    Citation
    Carr A, Samaras K, Burton S, Law M, Freund J, Chisholm DJ, Cooper DA. A syndrome of peripheral lipodystrophy, hyperlipidaemia and insulin resistance in patients receiving HIV protease inhibitors. AIDS. 1998 May 7;12(7):F51-8. doi: 10.1097/00002030-199807000-00003.
    Results Reference
    background
    PubMed Identifier
    10708054
    Citation
    Mulligan K, Grunfeld C, Tai VW, Algren H, Pang M, Chernoff DN, Lo JC, Schambelan M. Hyperlipidemia and insulin resistance are induced by protease inhibitors independent of changes in body composition in patients with HIV infection. J Acquir Immune Defic Syndr. 2000 Jan 1;23(1):35-43. doi: 10.1097/00126334-200001010-00005.
    Results Reference
    background
    PubMed Identifier
    16231263
    Citation
    Wohl DA, Tien HC, Busby M, Cunningham C, Macintosh B, Napravnik S, Danan E, Donovan K, Hossenipour M, Simpson RJ Jr. Randomized study of the safety and efficacy of fish oil (omega-3 fatty acid) supplementation with dietary and exercise counseling for the treatment of antiretroviral therapy-associated hypertriglyceridemia. Clin Infect Dis. 2005 Nov 15;41(10):1498-504. doi: 10.1086/497273. Epub 2005 Oct 11.
    Results Reference
    background

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    Omega-3 Supplementation in HIV Patients With Therapeutic Lifestyle Change Diet.

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