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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.
Register: PACTR
Last refreshed on: 29 April 2013
Main ID:  PACTR201301000445375
Date of registration: 26/10/2012
Primary sponsor: Damalie Nakanjako
Public title: Atorvastastin and HIV associated immune activation
Scientific title: Use of Atorvastatin among HAART-treated adults with suboptimal immune recovery in Uganda
Date of first enrolment: 2012-12-10
Target sample size: 30
Recruitment status: Open to recruitment: actively recruiting participa
URL:  HTTP://www.pactr.org/ATMWeb/appmanager/atm/atmregistry?da=true&tno=PACTR201301000445375
Study type:  interventional
Study design:  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,
 
Countries of recruitment
South Africa
Contacts
Name: Francis  Codero
Address:  3rd parklands avenue 30270-00100 Nairobi Kenya
Telephone: +254722449575
Email: Fcodero@yahoo.com
Affiliation:  Prin
Name: Francis  Codero
Address:  3rd parklands avenue 30270-00100 Nairobi Kenya
Telephone: +254722449575
Email: Fcodero@yahoo.com
Affiliation:  Principal investigator
Key inclusion & exclusion criteria
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
Health Condition(s) or Problem(s) studied

null
Intervention(s)
Primary Outcome(s)
Time to first request of analgesia following surgery
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
Aga Khan University Hospital
Secondary Sponsor(s)
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