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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05282849
Other study ID # SMS2022-1
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 4, 2022
Est. completion date June 15, 2022

Study information

Verified date April 2022
Source Cairo University
Contact Sherif M. Soaida, MD
Phone +201223663504
Email sherif_soaida@kasralainy.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Comparison between ultrasound guided transmuscular QL block and Fascia iliaca block in pediatric patients undergoing DDH surgery regarding the quality of pain control in the perioperative period..


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date June 15, 2022
Est. primary completion date June 1, 2022
Accepts healthy volunteers No
Gender All
Age group 2 Years to 12 Years
Eligibility Inclusion Criteria: - Children aged 2-12 years - Of both sexes - American society of anesthesiologist (ASA) physical status classification class I - Undergoing general anaesthesia for DDH surgery Exclusion Criteria: - Parents' refusal of regional block - Duration of surgery over 120 min. - History of allergy to local anesthetics - Bleeding disorders (INR >1.4, Platelet count< 75000)

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
ultrasound guided fascia iliaca block
ultrasound guided fascia iliaca block anesthetizes variable combinations of the femoral nerve , lateral femoral cutaneous nerve , and obturator nerve, and is effective for many painful hip surgeries making it potentially useful for analgesia following Developmental Dysplasia of Hip (DDH) surgery.
ultrasound guided quadratus lumborum block
ultrasound-guided quadratus lumborum (QL) block provides perioperative somatic, even visceral analgesia for patients including pediatrics, undergoing abdominal or hip surgery. The local anesthetic injected adjacently into the quadrates lumborum muscle spreads in a medial and cranial direction under the crura and arcuate ligaments of the diaphragm, then into the thoracic paravertebral space anesthetizing the hip region

Locations

Country Name City State
Egypt Faculty of medicine Cairo university Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Total 12 hours postoperative opioid consumption amount of morphine consumed as rescue analgesia in first 12 hours from the time of transfer of the patient to the pacu at one hour intervals for 12 hours
Secondary Postoperative pain using Face, Legs, Activity, Cry, Consolability scale (FLACC ) pain rating scale pain score of paitients in the post operative period from the time of transfer to the PACU, every hour for the first 24 hours postoperative]
Secondary Side effects respiratory depression and postoperative nausea and vomiting from the time of transfer to the PACU, for the first 24 hours postoperative
Secondary Total 24 hours postoperative opioid consumption amount of morphine consumed as rescue analgesia in first 24hours from the time of transfer of the patient to the pacu at one hour intervals for 24hours
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