HIV, Acquired Immunodeficiency Syndrome (AIDS) Infections and Infestations Human immunodeficiency virus (HIV)
Conditions
Interventions
Co-trimoxazole/desensitisation/direct rechallenge
Sponsors
Medical Research Council (MRC) (UK)
Eligibility
Inclusion criteria
Inclusion criteria: 1. Past or current severe reactions to co-trimoxazole 2. Other severe skin conditions 3. Creatinine above 250 micromoles/l, Alanine Aminotransferase (ALT)/Aspartate Aminotransferase (AST) above five times local limit 4. Haemoglobin below 10.5 g/dl, neutrophils below 0.75, platelets below 50
Exclusion criteria
Exclusion criteria: Not provided at time of registration
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Proportion of patients still taking co-trimoxazole four and 24 weeks after trial entry | — |
Secondary
| Measure | Time frame |
|---|---|
| Not provided at time of registration | — |
Countries
United Kingdom
Outcome results
None listed