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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06391528
Other study ID # 2024/06-19
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date April 1, 2024
Est. completion date June 30, 2025

Study information

Verified date April 2024
Source Zonguldak Bulent Ecevit University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

to investigate the effects of Transversalis Fascia Plan Block after induction of anesthesia on perioperative opioid consumption, hemodynamic changes, postoperative FLACC pediatric pain score, non-opioid analgesic use and parental satisfaction in pediatric patients undergoing unilateral inguinal hernia or undescended testicular repair under general anesthesia.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 60
Est. completion date June 30, 2025
Est. primary completion date April 30, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 1 Year to 9 Years
Eligibility Inclusion Criteria: - 1-9 years old - ASA I-II risk group - Patients whose consent was obtained from their parents with an informed consent form - Patients who will undergo Inguinal Hernia or Undescended Testi Exclusion Criteria: - ASA >2 - History of allergy to local anesthetics - Known coagulation disorders - Infection near the entry site - Body mass index >30 - Those whose parents refused to participate in the study - Those contraindicated for regional anesthesia - Those with neurological or neuromuscular disease - Patients with psychiatric problems - Patients with a history of opioid use - Chronic analgesic use - Operation duration exceeding 2 hours

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Transversalis Fascia Plane Block
application of local anesthetic between the transversus abdominis muscle and the transversalis fascia surrounding it from the inside, at the level of the posterior axillary line.

Locations

Country Name City State
Turkey Zonguldak Bülent Ecevit University medicine faculty Zonguldak Kozlu

Sponsors (1)

Lead Sponsor Collaborator
Zonguldak Bulent Ecevit University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary postoperative pain scores Patients will be evaluated at regular intervals after surgery and their pain will be measured using a FLACC scores. up to 24 hour after surgery
Secondary parental satisfaction asking parents about their satisfaction during the procedure
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