Trial · NCT01402882
Registered outcomes12
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 12 of 12
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | The primary outcome is death in hospital in patients recruited within 3 hours and cause of death will be described. | within 28 days of injury | |
| Secondary | (a) Vascular occlusive events (myocardial infarction, stroke, pulmonary embolism, clinical evidence of deep vein thrombosis) | Prior death, discharge or 28 days | |
| Secondary | (b) In hospital disability assessed using the Disability Rating Scale and Patient Orientated Outcome | Prior death, discharge or 28 days | |
| Secondary | (c) Seizures | Prior death, discharge or day 28 | |
| Secondary | (d) Neurosurgical intervention | prior death, discharge or day 28 | |
| Secondary | (e) Days in intensive care | prior death, discharge or day 28 | |
| Secondary | (f) Other adverse events | prior death, discharge or day 28 | |
| Other | CRASH-3 IBS: Primary outcome - the total volume of intracranial haemorrhage | 1) CT scan done before receipt of trial treatment; (2) CT scan done after receipt of trial treatment (up to 28 days after randomisation) | |
| Other | Frequency of progressive haemorrhage: number of patients with a post-randomisation CT scan with total haemorrhage volume of more than 25% of the volume on the pre-randomisation scan | 1) CT scan done before receipt of trial treatment; (2) CT scan done after receipt of trial treatment (up to 28 days after randomisation) | |
| Other | Frequency of delayed haemorrhage: | 1) CT scan done before receipt of trial treatment; (2) CT scan done after receipt of trial treatment (up to 28 days after randomisation) | |
| Other | New focal ischaemic lesions: | 1) CT scan done before receipt of trial treatment; (2) CT scan done after receipt of trial treatment (up to 28 days after randomisation) | |
| Other | • Total volume of intracranial bleeding in patients who undergo surgical evacuation of haemorrhage after randomisation | 1) CT scan done before receipt of trial treatment; (2) CT scan done after receipt of trial treatment (up to 28 days after randomisation) |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
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
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT01402882/registered