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NCT00643032 Clinical Trial

Preoperative Anxiety and Postoperative Pain in Children

Post-Operative Pain Clinical Trial

Official title:
Comparison of 2 Methods to Reduce Postoperative Pain in Children and a Comparison of 3 Methods of Preoperative Education Intervention to Reduce Anxiety in Children and Their Family

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

Related Conditions & MeSH terms

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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