Autopsy report · NCT05624359
Flurbiprofen Axetil as an Adjuvant to Pre-emptive Scalp Infiltration
Cause of deathStaffing, sites or logistics
“One case with postoperative subdural hematoma was reported to the Institutional Review Board and DMC. This study was suspended. The association with study interventions remained to be explored.”
Life of this trial
- Registered 1 year before it started.
- Suspended: paused, and may or may not restart.
- 216 participants planned (an estimate, not an actual count).
Vital statistics
- Status
- Suspended
- Phase
- Na
- Sponsor
- Beijing Tiantan Hospital
- Sponsor type
- University, hospital or other
- Conditions
- Postoperative Pain
- Interventions
- FA plus ropivacaine; ropivacaine alone
- Participants
- 216 (planned, not actual)
- Sites
- 1
- Countries
- China
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.