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NCT01684774 Clinical Trial

Comparison Between Ultrasound-guided and Landmark-guided Ankle Blocks

Analgesia Clinical Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT01684774
Other study ID # 0070-12-HYMC
Secondary ID
Status Not yet recruiting
Phase N/A
First received September 10, 2012
Last updated September 12, 2012
Start date December 2012
Est. completion date December 2014

Study information
Verified date September 2012
Source Hillel Yaffe Medical Center
Contact Leonid Reytman, MD
Phone 972-54-4226640
Email lrey@netvision.net.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

The investigators will be comparing ultrasound-guided (USG) ankle block and anatomic landmark-guided (ALG) ankle block to determine which of these procedures is better in surgical anesthesia and in postoperative pain relief.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 100
Est. completion date December 2014
Est. primary completion date December 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients undergoing orthopedic foot operation with osteotomy

Exclusion Criteria:

- Skin infection near block injection site

- Allergy to local anesthetics

- Coagulopathy with INR >1.4.

- Dementia

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Drug:
• Bupivacaine

Locations
Country Name City State
Israel Hillel Yaffe Medical Center Hadera

Sponsors (1)
Lead Sponsor Collaborator
Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary Surgical Anesthesia Sufficient Sufficiency of surgical anesthesia will be determined by the presence of a complete sensory or motor block. If general anesthesia needs to be added to achieve operative analgesia, the surgical block will not be deemed sufficient. Thirty minutes No
Primary Post-operative Pain Relief Intensity of post-operative pain will be measured by a numerical scale from 0-10 by the patient Twenty-four hours No
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