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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: |
PACTR201301000445375 |
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Date of registration:
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26/10/2012 |
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Primary sponsor: |
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Public title:
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Atorvastastin and HIV associated immune activation
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Scientific title:
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Use of Atorvastatin among HAART-treated adults with suboptimal immune recovery in Uganda |
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Date of first enrolment:
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2012-12-10 |
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Target sample size:
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30 |
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Recruitment status: |
Open to recruitment: actively recruiting participa |
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URL:
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HTTP://www.pactr.org/ATMWeb/appmanager/atm/atmregistry?da=true&tno=PACTR201301000445375 |
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Study type:
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interventional |
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Study design:
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Crossover: all participants receive all interventions in different sequence during study, Randomised, simple randomisation using a randomisation table created by a computer software program, sealed opaque envelopes,
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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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Francis
Codero |
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Address:
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3rd parklands avenue
30270-00100
Nairobi
Kenya |
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Telephone:
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+254722449575 |
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Email:
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Fcodero@yahoo.com |
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Affiliation:
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Prin |
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Name:
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Francis
Codero |
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Address:
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3rd parklands avenue
30270-00100
Nairobi
Kenya |
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Telephone:
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+254722449575 |
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Email:
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Fcodero@yahoo.com |
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Affiliation:
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Principal investigator |
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Key inclusion & exclusion criteria
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Inclusion criteria: ASA I and II patients scheduled for lower limb orthopaedic surgery
Exclusion criteria: 1. Patient refusal
2. Patients `18years and b76years
3.Failure to reach the sub arachnoid space and converted to GA
4.Patients with contraindications to neuraxial anaesthesia
Puncture site infection
Hypovolemic shock
c. Coagulopathy
d. Sepsis
5. Patients with psychological / mental instability
6. Patients with known psychiatric condition
7. Patient involved in any other clinical studies
Age minimum:
18 Year
Age maximum:
75 Year
Gender:
Both
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Health Condition(s) or Problem(s) studied
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null
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Primary Outcome(s)
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Time to first request of analgesia following surgery
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Source(s) of Monetary Support
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Aga Khan University Hospital
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