Amantadine to Speed Awakening After Cardiac Arrest
Completed · Phase 2 · Has a placebo group
Conditions studied: Coma, Heart Arrest, Anoxia
In brief
This study evaluates if amantadine will increase the rate of awakening in patients resuscitated from cardiac arrest but comatose (not following commands) after their resuscitation. Half of the participants will receive amantadine and the other will receive placebo.
Key facts
- Study ID
- NCT02486211
- Run by
- Jon Rittenberger, MD
- People needed
- 14
- Starts
- 2015-09-01
- Expected to finish
- 2018-06-30
- Last updated by the study team
- 2019-12-04
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Non traumatic cardiac arrest
- Age 18 and older
- Defibrillation and/or chest compressions by healthcare providers
- Return of spontaneous circulation
You may not qualify if…
- Written do not attempt resuscitation (DNAR) reported to providers before randomization
- Known prisoner or pregnancy
- Lack of motor response to pain and absent N20 response on somatosensory evoked potentials prior to randomization
- Initial CT demonstrating brain edema (defined as grey white ratio <1.2)
- Presence of malignant pattern on EEG at time of randomization
- Next of kin unwilling to provide supportive care for at least one week after enrollment
- Presently using other dopaminergic agent
Where it is running
- Main Medical Center — Portland, Maine, United States
- Beth Israel Deacconness — Boston, Massachusetts, United States
- UPMC Presbyterian Hospital — Pittsburgh, Pennsylvania, United States
- UPMC Mercy Hospital — Pittsburgh, Pennsylvania, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.