NCT Number: NCT01245868
Spinal Anaesthesia for Knee Arthroscopy: Does Lignocaine Shorten the Effect of Bupivacaine
The purpose of the study is to investigate if a small amount of lignocaine added to bupivacaine for spinal anesthesia to patients planned for arthroscopic knee surgery, can shorten the duration of the sensoric and the motoric blockade.
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Notify MeKey information
Conditions
Age range
18 year–65 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
Primary location
Dep. of anesthesiology, Hospital of Frederikssund, Frederikssund, Denmark
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- The patient want spinal anaesthesia
- No contradictions against spinal anaesthesia
- Healthy people (ASA-score 1 or 2)
- Body mass index < 35 and between 155 and 190 cm
Exclusion criteria
- Known allergic reactions to planned drugs
- Neurologic disturbances
- Diabetes
Treatment and study plan
Bupivacaine
DrugPrimary outcomes
-
Duration of spinal blockade
Time frame: Repeating monitoring every 15 minutes after applying the blockade, up to 360 minutes.
Secondary outcomes
-
Time to fulfillment of discharge criteria from the hospital.
Time frame: Evaluated every 15 minutes after the operation up to 360 minutes. On average 200 to 300 minutes.
Sponsors and collaborators
Lead sponsor
Frederikssunds Hospital, Denmark
Other
Registry information
Official study title
Spinal Anaesthesia for Knee Arthroscopy: Does Lignocaine Shorten the Effect of Bupivacaine?
Important dates
- Study start
- 2009
- Primary completion
- 2010
- Study completion
- 2010
- First posted
- Nov 23, 2010
- Registry last updated
- May 8, 2015
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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