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Intervention (protocolized clonidine initiation) for Substance Withdrawal
Study Summary
This trial tests if a drug can reduce symptoms, shorten hospital stays, and reduce costs for sedation in the hospital.
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- You have a history of mental health issues.You are taking alpha-2 agonist medications at home.People who have died while taking dexmedetomidine.You have been receiving dexmedetomidine continuously for 3 or more days.
- Group 1: Usual care (without protocolized clonidine initiation)
- Group 2: Intervention (protocolized clonidine initiation)
- Drug Has Already Been Approved - The FDA has already approved this drug, and is just seeking more data.
- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
Has the FDA sanctioned Intervention (protocolized clonidine initiation) for usage?
"Having already been approved, the safety score of Intervention (protocolized clonidine initiation) was assigned a 3 on Power's scale. This is due to this treatment falling under Phase 4 trial status."
Is there an open recruitment period for participants in this research?
"Per the information posted on clinicaltrials.gov, this medical study is not actively recruiting patients at this time. The trial was initially shared on October 31st 2022 and saw its last update seven days later; despite that though, there are other similar experiments searching for participants as we speak."
Who would be the ideal participants for this medical investigation?
"In this research project, 300 participants aged between 4 weeks and 18 years who have been receiving Dexmedetomidine infusion for over 72 hours are eligible."
Are individuals aged 45 or older being deemed eligible for this research project?
"This medical investigation is seeking participants aged between 4 weeks and 18 years."
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