Status:
COMPLETED
Intraoperative Intravenous Lidocaine
Lead Sponsor:
Federal University of São Paulo
Conditions:
Pain Intensity
Eligibility:
FEMALE
18-60 years
Phase:
NA
Brief Summary
The objective of the present study was to evaluate the effect of intraoperative intravenous lidocaine on postoperative pain after hysterectomy.
Detailed Description
Study design A prospective, randomized, double-blind study was conducted according to ethical guidelines for research involving humans. The study was approved by the Ethics Committee of the institutio...
Eligibility Criteria
Inclusion
- ASA 1 or 2, aged 18 to 60 years undergoing hysterectomy
Exclusion
- Cardiac arrhythmia; myocardiopathy
- Altered cardiac conduction
- Psychiatric, hepatic or respiratory disease
- Patients receiving any type of analgesic during the week before surgery
Key Trial Info
Start Date :
May 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2008
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT00965796
Start Date
May 1 2008
End Date
December 1 2008
Last Update
August 26 2009
Active Locations (2)
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1
Rioko K Sakata- Universidade Federal de São Paulo
São Paulo, Rua Botucatu-593, Brazil, 04023-062
2
Universidade Federal de São Paulo
São Paulo, São Paulo, Brazil, 04023-062