Completed

IMMUNEImmune Enhancement for Immunological Non-responders to ART

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What is being tested

Zinc and SAMe

Dietary Supplement
Who is being recruted

Over 21 Years
See all eligibility criteria
How is the trial designed

Other Study

Interventional
Study Start: March 2013
See protocol details

Summary

Principal SponsorEmory University
Last updated: July 18, 2019
Sourced from a government-validated database.Claim as a partner

Study start date: March 1, 2013

Actual date on which the first participant was enrolled.

There will be up to eleven study visits and three telephone visits. All study procedures are for research purposes. All study subjects will receive the nutritional supplements zinc and SAMe. During the study you will be asked to answer questions about your alcohol use and smoking history. You will have exhaled breath tests, blood draws, physical exams, and bronchoscopies. Your medical records will be reviewed during the study. If you are a woman of childbearing age, a urine pregnancy test will be done at each study visit. Visit 1 (screening visit): This visit will last about 2 hours. At this visit you will: Have a physical exam Review your medical history Review your medications Have blood drawn Have a urine pregnancy test for women of child-bearing age Complete a survey about your alcohol use and smoking history. Discuss and schedule a bronchoscopy for the next visit You may not be eligible to continue in the study if the blood work done at visit one is not within normal limits or if you are pregnant. A study team member will contact you to let you know if you do or do not qualify to participate in the remainder of the study. Visit 2: This visit will last about 6 hours and will take place at the Hospital. At this visit you will: Have a physical exam Have blood drawn Have a urine pregnancy test for women of child-bearing age Do an exhaled breath test Have a bronchoscopy Receive nutritional supplements and education Treatment: The nutritional supplements zinc and SAMe will be given to you by the study team at visit 2. You will be asked to take the tablets once a day. If you experience upset stomach, abdominal cramps, diarrhea, or other uncomfortable side effects, we will reduce the amount of the nutritional supplements. If you are unable to tolerate the nutritional supplements, you will be withdrawn from the research study. Visits 3, 4, and 5 -Telephone Contact: You will receive a telephone call at one, two, and three weeks after visit 2 to ask you how you are tolerating the study supplements. If you are experiencing side effects such as upset stomach, abdominal cramps, or diarrhea, we will instruct you to decrease the dose of the supplements. Visits 6, 7, and 8 (months one, two, and three): These visits will last about 30 minutes and will be scheduled two months apart. At this visit you will: Have blood drawn Have a urine pregnancy test for women of child-bearing age Do an exhaled breath test Answer questions about how you are tolerating the nutritional supplements Receive nutritional supplements and education If your exhaled breath test is at goal at visit 6, you will continue to take the dietary supplements for one year from this point forward. If your exhaled breath test is not at goal at visit 6, you will be asked to return for visit 7. If your exhaled breath test is at goal at visit 7, you will continue to take the dietary supplements for one year from this point forward. If your exhaled breath test is not at goal at visit 7, you will be asked to return for visit 8. You will be asked to take the nutritional supplements for one year from this point forward. Visits 9 through 13: These visits will last about 30 minutes and will be scheduled two months apart. At this visit you will: Have blood drawn Have a urine pregnancy test for women of child-bearing age Answer questions about how you are tolerating the nutritional supplements Receive nutritional supplements and education Visit 14: This is the final study visit. It will last about 6 hours and will take place at the Hospital. At this visit you will: Have a physical exam Have blood drawn Have a urine pregnancy test for women of child-bearing age Do an exhaled breath test Have a bronchoscopy procedure Return unused nutritional supplements

NCT01806870
Principal SponsorEmory University
Last updated: July 18, 2019
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

30 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Other Study

Some studies explore topics that don't fall into a specific category. These might include innovative research, new technologies, or emerging healthcare areas.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 21 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

Inclusion Criteria: 1. Subjects living with HIV-1 infection who have been on anti-retroviral therapy (ART) for a minimum of 18 months and: are followed longitudinally for their HIV healthcare in one of the study sites in Atlanta or Seattle meet criteria for immunological non-responsiveness as defined by adherence to ART and cluster of differentiation 4 (CD4) count <350 despite adequate retroviral suppression. 2. Ability to give informed consent. Exclusion Criteria: Documented history of cirrhosis or a total bilirubin ≥ 2.0 mg/dL. Documentation of left ventricular ejection fraction < 40% or myocardial infarction within the past 6 months. End-stage renal disease requiring dialysis or a serum creatinine ≥ 2 mg/dL. Spirometry with Forced vital capacity (FVC) or Forced expiratory volume in 1 second (FEV1) < 70% of predicted value. Diabetes Known or possible pregnancy or attempting to become pregnant. BMI < 17 Age < 21 Parkinson's disease: these are all b/c the SAMe risks sections states that these pts will not qualify Bipolar disorder Bleeding disorders such as thrombocytopenia or significant gastrointestinal bleeding within the past year

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Each subject will receive 1600mg of SAMe per day Men subjects will receive 30mg Zinc Women subjects will receive 25mg Zinc

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 2 locations

Grady Hospital- Ponce De Leon Clinic

Atlanta, United StatesOpen Grady Hospital- Ponce De Leon Clinic in Google Maps

Atlanta VA Medical Center

Decatur, United States
Completed2 Study Centers