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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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PACTR |
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Last refreshed on:
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29 April 2013 |
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Main ID: |
PACTR201007000226131 |
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Date of registration:
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20/06/2010 |
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Primary sponsor: |
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Public title:
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COMPARISM BETWEEN ONCE DAILY AND TWICE DAILY LPV/RTR CO-ADMINISTERED WITH TENOFOVIR AND EMTRICITOBIN AMONG HIV INFECTED PATIENTS DURING MUSLIM RAMADAN
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Scientific title:
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COMPARISM BETWEEN ONCE DAILY AND TWICE DAILY LPV/RTR CO-ADMINISTERED WITH TENOFOVIR AND EMTRICITOBIN AMONG HIV INFECTED PATIENTS DURING MUSLIM RAMADAN FASTING. |
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Date of first enrolment:
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2010-07-20 |
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Target sample size:
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100 |
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Recruitment status: |
Not yet recruiting |
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URL:
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HTTP://www.pactr.org/ATMWeb/appmanager/atm/atmregistry?da=true&tno=PACTR201007000226131 |
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Study type:
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interventional |
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Study design:
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Parallel: different groups receive different interventions at same time during study,
Randomised,
simple randomisation using a randomisation table from a statistic book.,
Allocation was determined by the holder of the sequence who is situated off site,
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Countries of recruitment
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South Africa
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Contacts
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Name:
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AM
Yakasai |
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Address:
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Dept. of Medicine AKTH, Kano
234
Kano
Nigeria |
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Telephone:
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+2348065419097 |
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Email:
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amyakasai@yahoo.com |
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Affiliation:
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Senior registrar Infectious and Tropical Diseases |
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Name:
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Muhammad
Hamza |
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Address:
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Dept. of Medicine AKTH, Kano
234
Kano
Nigeria |
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Telephone:
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+2348035053139 |
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Email:
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drhamza1020@ymail.com |
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Affiliation:
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Senior registrar Infectious and Tropical Diseases |
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Key inclusion & exclusion criteria
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Inclusion criteria: -age above 18 years
- clinically stable
-patint should be on Tenofovir + Emtricytobin+ Lopinavir/ritonavir.
-patient that consented.
Exclusion criteria: -Less than 18 year
-patient on other ARV regimen
-patient that refuse to consent.
Age minimum:
18 Year
Age maximum:
70 Year
Gender:
Both
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Health Condition(s) or Problem(s) studied
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HIV/AIDS
null
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Primary Outcome(s)
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Adherence
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Laboratory monitoring(Lipid profile, Kidney function test, haematocrit)
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Therapeutic drug monitoring
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Tolerability(Presence or Abscence of adverse drug effects)
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Secondary Outcome(s)
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Effectiveness(Viral load, CD4 count)
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Source(s) of Monetary Support
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Institute of human virology, Kano region -Nigeria
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