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NCT00721110 · ClinicalTrials.gov registry record · NA
Lidocaine and Ketamine in Abdominal Surgery
A NA study, sponsored by The Cleveland Clinic.
- Terminated
- Registry status
- NA
- Development phase
- 64
- Enrollment target
NCT00721110 is a NA study that was terminated before completion, run by The Cleveland Clinic. The registered enrollment target is 64 participants.
The verdict
NCT00721110, a NA study, was terminated before completion, sponsored by The Cleveland Clinic.
- TERMINATED
- Registry status
- NA
- Development phase
- 64 participants
- Enrollment target
Study Summary
This study is being done to determine if combined infusions of lidocaine and ketamine is better than a lidocaine or ketamine infusion alone, or to placebo in improving recovery after abdominal hysterectomy. Participants will be randomized into one of four groups. Evaluations will be done through walking tests, pain and fatigue questionnaires and blood tests.
Interventions
- DRUG Placebo
- DRUG Ketamine
- DRUG Lidocaine
- DRUG Ketamine + Lidocaine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 64 participants |
| Start Date | 2008-07 |
| Est. Completion | 2012-07 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00721110
The ClinicalTrials.gov registry entry for NCT00721110 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 64 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The Cleveland Clinic, which has 688 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 4 interventions - of which Placebo is the first listed.
NCT00721110 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00721110 about?
NCT00721110 is a clinical study titled "Lidocaine and Ketamine in Abdominal Surgery". This study is being done to determine if combined infusions of lidocaine and ketamine is better than a lidocaine or ketamine infusion alone, or to placebo in improving recovery after abdominal hysterectomy. Participants will be randomized into one of four groups. Evaluations will be done through wal...
What is the current status of trial NCT00721110?
This trial is currently terminated. It is a NA study. The enrollment target is 64 participants. The study started on 2008-07. Estimated completion is 2012-07.
What interventions are being tested in trial NCT00721110?
The interventions under investigation include: Placebo (DRUG), Ketamine (DRUG), Lidocaine (DRUG), Ketamine + Lidocaine (DRUG).
Who is sponsoring clinical trial NCT00721110?
This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.
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