BridgeMD
New treatment option for Cardiac Arrest
Official title Neuroprotection Bundles For Comatose Survivors Following Cardiac Arrest
ClinicalTrials.gov ID: NCT06992843
What this study is testing
- What it's testing
- The investigators designed LAPTOPS to determine the effectiveness of a goal-directed neuroprotection bundles of active management including body temperature,PaCO2,PaO2,position,Blood glucose ,blood sodium,Blood pressure and Lactate vs. usual care in adult post-cardiac arrest care.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 80
You may be able to join if
- Age ≥ 18 years and \< 80 years
- Patients of in-hospital or out-of-hospital cardiac arrest who have returned -spontaneous circulation (ROSC) after cardiopulmonary resuscitation and...
- Patients who are unconscious after ROSC, defined as FOUR motor response score \< 4 points or GSC ≤ 8 points;
- Family members or legal representatives signed informed consent.
You likely can't join if
- Unwitnessed cardiac arrest, estimated time from cardiac arrest to start of CPR \> 30 minutes;
- Time from cardiac arrest to ROSC \> 60 minutes;
- Patients who woke up immediately after ROSC by CPR;
- End-stage diseases;
- Cardiac arrest considered to be caused by neurological diseases;
- The patient was in a vegetative state before cardiac arrest;
See the full eligibility criteria
- Age ≥ 18 years and \< 80 years
- Patients of in-hospital or out-of-hospital cardiac arrest who have returned -spontaneous circulation (ROSC) after cardiopulmonary resuscitation and do not require CPR for more than 20 minutes;
- Patients who are unconscious after ROSC, defined as FOUR motor response score \< 4 points or GSC ≤ 8 points;
- Family members or legal representatives signed informed consent.
- Unwitnessed cardiac arrest, estimated time from cardiac arrest to start of CPR \> 30 minutes;
- Time from cardiac arrest to ROSC \> 60 minutes;
- Patients who woke up immediately after ROSC by CPR;
- End-stage diseases;
- Cardiac arrest considered to be caused by neurological diseases;
- The patient was in a vegetative state before cardiac arrest;
- The interval from the onset of cardiac arrest to enrollment is \>72 hours .
The study team makes the final eligibility decision.
Where it's taking place
- Changsha, Hunan, China
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 80 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Changsha, Hunan, China. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.