CClinicalTrials.gg
Status unknownNCT00643032Updated Mar 25, 2008

Preoperative Anxiety and Postoperative Pain in Children

A Phase 4 interventional study of Transcutaneous iliohypogastric and Perioperative administration near the nerve in Post-Operative Pain and Pre-Operative Anxiety, sponsored by Hillel Yaffe Medical Center. Status unknown at 1 site in Israel. Open to participants aged 3 Months to 12 Years. Per ClinicalTrials.gov, last updated 2008-03-25.

Sponsored by Hillel Yaffe Medical Center · Phase 4, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Mar 2008), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Phase 4
Study type
Interventional
Enrollment
250
Allocation
Randomized
Ages
3 Months to 12 Years
Sex
All
01

Study 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.

02

Conditions studied

  • Post-Operative Pain
  • Pre-Operative Anxiety
03

In context

Pain, Postoperative

5,093 studies on the registry are indexed under Pain, Postoperative; 1,140 are open to participants now.

This study's planned enrollment of 250 is above the median of 75 across 4,344 interventional studies indexed under Pain, Postoperative.

Browse Pain, Postoperative studies →

Lead sponsor

Hillel Yaffe Medical Center is the lead sponsor of 301 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
3 Months to 12 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Healthy
  • ASA I - II
  • Undergoing elective day surgery

Exclusion criteria

Exclusion Criteria:

  • Known coagulation dysfunction
  • Sensitivity to analgesics
05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Enrollment
250 participants (estimated)

Study arms

  • Active comparator
    I

    Procedure: Transcutaneous iliohypogastric

  • Active comparator
    II

    Procedure: Perioperative administration near the nerve

Interventions

  • ProcedureTranscutaneous iliohypogastric
  • ProcedurePerioperative administration near the nerve
06

Study locations

1 site
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 25, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00643032
Lead sponsor
Hillel Yaffe Medical Center
First posted
Mar 25, 2008
Start date
Mar 2008
Primary completion
Jan 2010 (estimated)
Last update
Mar 25, 2008

Study contacts

Zvi Steiner, MD
Contact
steiner@hy.health.gov.il
972-4-6304434

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Mar 2008. You cannot join it, but the record below documents what was studied.

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