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An open label observational clinical study to compare the efficacy of EMLA cream (lidocaine 2.5% and prilocaine 2.5% in a ratio of 1:1 by weight) in comparison to the established local anesthesia (LA) protocol of lidocaine subcutaneous injection, in providing adequate peri-operative local anesthesia during transradial coronary angiography
A total of 800 consecutive patients, who are referred for elective coronary angiography to 1st Cardiology Department cathlab, with the suspicion of coronary artery disease (CAD) will be enrolled in this study. Exclusion criteria are acute coronary syndrome, previous ipsilateral transradial approach, Raynaud's syndrome, abnormal renal function with or without need for hemodialysis, known history of sensitivity to local anesthetics, non-palpable radial pulse, abnormal Barbeau's test and patient's refusal. Baseline clinical, demographic and procedural data of the study population will be recorded.
The study will not involve any intervention but it will observe patients assigned to other EMLA cream or lidocaine injection for local anesthesia as part of their clinical routine treatment during transradial catherization.
Primary end-point: the perception of radial pain assessed during artery puncture and 30 minutes after sheath removal. Secondary end-point: The number of puncture attempts, the total time required before successful sheath insertion, and the occurrence of radial artery spasm will be also documented in each group Participants will be observed for 4 hours post angiography for development of local complications or side effects.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| EMLA anesthetic ointment (AO) | In AO group a layer of 2.5 gr EMLA cream (standard adult dose) is applied to both wrists, 1 cm above the styloid process of the radius 30 minutes before the puncture, by an experienced cathlab nurse | ||
| Local Skin Anesthetic Injection (LA) | In LA group the radial artery is infiltrated with 1-2 mL of 2% lidocaine, using a 26 G needle, 0.5-1 cm proximal to the styloid process one minute before the puncture |
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| Measure | Description | Time Frame |
|---|---|---|
| Visual Analog Scale of Pain Perception during sheath insertion | The primary end-point of the study is the perception of radial pain assessed during artery puncture | During artery puncture |
| Measure | Description | Time Frame |
|---|---|---|
| Puncture efficiency | The total time required for successful sheath insertion is documented in each group and constitutes the secondary end point of the study assessing puncture efficiency | During radial artery catheterization |
| Radial artery spasm |
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Inclusion Criteria:
- patients, referred for elective diagnostic coronary angiography
Exclusion Criteria:
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A total of 800 consecutive patients, referred for elective coronary angiography In 1stCardiology Dpt Cath Lab with the suspicion of coronary artery disease (CAD) are enrolled in this study. All procedures will be undertaken by experienced and radial dedicated interventional cardiologists (i.e. more than 90% radial catheterizations). Exclusion criteria were acute coronary syndrome, previous ipsilateral transradial approach, Raynaud's syndrome, abnormal renal function with or without need for hemodialysis, known history of sensitivity to local anesthetics, non-palpable radial pulse, abnormal Barbeau's test and patient's refusal
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| Name | Affiliation | Role |
|---|---|---|
| Dimitris Tousoulis, MD PhD | 1st Cardiology Department - Athens Medical School | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| 1st Cardiology Department Hippokration Hospital | Athens | Attica | 11528 | Greece |
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The occurrence of radial artery spasm in each group during radial artery catheterization
| During radial artery catheterization |
| Visual Analog Scale of Pain Perception 30 minutes after sheath removal | The primary end-point of the study is the perception of radial pain assessed 30 minutes after sheath removal | 30 minutes after sheath removal |