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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT00643032
Other study ID # 50/2007
Secondary ID
Status Not yet recruiting
Phase Phase 4
First received March 19, 2008
Last updated March 19, 2008
Start date March 2008

Study information

Verified date March 2008
Source Hillel Yaffe Medical Center
Contact Zvi Steiner, MD
Phone 972-4-6304434
Email steiner@hy.health.gov.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

We wish to study which method of local injection of analgesic (before or during surgery) is the more effective method to reduce post-operative pain in children. In addition, we wish to study which pre-operative educational intervention is more effective in reducing anxiety in children and their family.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 250
Est. completion date
Est. primary completion date January 2010
Accepts healthy volunteers No
Gender Both
Age group 3 Months to 12 Years
Eligibility Inclusion Criteria:

- Healthy

- ASA I - II

- Undergoing elective day surgery

Exclusion Criteria:

- Known coagulation dysfunction

- Sensitivity to analgesics

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Primary Purpose: Treatment


Intervention

Procedure:
Transcutaneous iliohypogastric

Perioperative administration near the nerve


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, 

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