Comparison · NCT03296553-deaths
Valganciclovir vs Antiretroviral Combinations: deaths from any cause
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. Valganciclovir vs Antiretroviral Combinations: deaths from any cause. Trial comparisons, record NCT03296553-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03296553-deaths
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.167 | 0.0584 | 0.392 | wilson | |
| Risk in group 2 | 0.158 | 0.0552 | 0.376 | wilson | |
| Risk difference, group 1 minus group 2 | 0.00877 | -0.234 | 0.257 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.06 | 0.244 | 4.57 | log | |
| Odds ratio, group 1 over group 2 | 1.07 | 0.186 | 6.13 | log | |
| Number needed to harm, for one more death from any cause on Valganciclovir than on Antiretroviral Combinations | 114 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Valganciclovir | Oral Valgancyclovir 900 mg twice in a day during 4 weeks prior to initiation of cART (combined antirretroviral therapy) until suppression of HHV-8.~Valganciclovir: The experimental group will receive Valganciclovir 900 mg twice in a day before the initiation of cART until viral load of HHV-8 is undetectable.~20 experimental included 2 eliminated~18 patients included finally. | 3 | 18 | EG000 |
| Group 2 | Antiretroviral Combinations | Standard treatment with cART according to current HIV Therapy Mexican guidelines.~Antiretroviral Combinations: Patients will receive standard antiretroviral treatment as recommended~20 control patients included~1 eliminated~19 patients included finally | 3 | 19 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, all-cause mortality
- Time frame
- 48 weeks
Source ClinicalTrials.gov
Trial
- Title
- Impact of Valganciclovir on Severe IRIS-Kaposi Sarcoma Mortality: an Open-label, Parallel, Randomized Controlled-trial.
- NCT number
- NCT03296553
- Phases
- PHASE2
- Conditions
- Kaposi Sarcoma, Human Immunodeficiency Virus, Immune Reconstitution Syndrome
- Interventions
- Valganciclovir, Antiretroviral Combinations
- Lead sponsor
- National Institute of Cancerología
- Results first posted
- 2022-01-27
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT03296553?tab=results
Source ClinicalTrials.gov
Source
- Release
- trial-comparisons-2026-03-23-0.1.0
- Release manifest SHA-256
- f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
- AACT copy
- 2026-03-23
- Tables read
- outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet
Source ClinicalTrials.gov
Sources 2
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.
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