Trials / Completed
CompletedNCT00975910
Effect of Lidocaine in Antiarrhythmic Dosage on Postoperative Cognitive Dysfunction in Supratentorial Craniotomy Dysfunction in Supratentorial Craniotomy
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 100 (actual)
- Sponsor
- Capital Medical University · Academic / Other
- Sex
- All
- Age
- 18 Years – 60 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to investigate the effect of lidocaine in antiarrhythmic dosage on postoperative cognitive dysfunction in supratentorial craniotomy.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | lidocaine | Lidocaine arm: lidocaine (2%) as an intravenous bolus (1.5 mg/kg) during induction followed by an intravenous infusion (2 mg. kg(-1).h(-1)) after induction until at the end of surgery |
| DRUG | saline | Saline arm: infused at the same rate as lidocaine |
Timeline
- Start date
- 2009-09-01
- Primary completion
- 2012-05-01
- Completion
- 2012-12-01
- First posted
- 2009-09-14
- Last updated
- 2013-05-22
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT00975910. Inclusion in this directory is not an endorsement.