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NCT00997113 · ClinicalTrials.gov registry record · Phase 4
Stress During Deep Sedation With Propofol With and Without Alfentanil
A Phase 4 study, sponsored by Hennepin Healthcare Research Institute.
- Completed
- Registry status
- Phase 4
- Development phase
- 20
- Enrollment target
NCT00997113 is a Phase 4 study that has completed, run by Hennepin Healthcare Research Institute. The registered enrollment target is 20 participants.
The verdict
NCT00997113, a Phase 4 study, has completed, sponsored by Hennepin Healthcare Research Institute.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 20 participants
- Enrollment target
Study Summary
This is a randomized clinical trial of deep procedural sedation with propofol with and without supplemental alfentanil. Patients will be assessed for total and fractionated serum catecholamines before and after the procedure in addition to usual procedural sedation outcomes parameters to assess the adrenergic effect of propofol sedation without supplemental opioid.
Interventions
- DRUG propofol
- DRUG alfentanil
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2009-10 |
| Est. Completion | 2012-12 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00997113
The ClinicalTrials.gov registry entry for NCT00997113 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Hennepin Healthcare Research Institute, which has 63 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which propofol is the first listed.
NCT00997113 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00997113 about?
NCT00997113 is a clinical study titled "Stress During Deep Sedation With Propofol With and Without Alfentanil". This is a randomized clinical trial of deep procedural sedation with propofol with and without supplemental alfentanil. Patients will be assessed for total and fractionated serum catecholamines before and after the procedure in addition to usual procedural sedation outcomes parameters to assess the ...
What is the current status of trial NCT00997113?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 20 participants. The study started on 2009-10. Estimated completion is 2012-12.
What interventions are being tested in trial NCT00997113?
The interventions under investigation include: propofol (DRUG), alfentanil (DRUG).
Who is sponsoring clinical trial NCT00997113?
This trial is sponsored by Hennepin Healthcare Research Institute, which has 63 total clinical trials registered on ClinicalTrials.gov.
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