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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04720287
Other study ID # FMASU MS 728/2020/2021
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date February 1, 2021
Est. completion date April 30, 2021

Study information

Verified date May 2021
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to compare the postoperative pain control in children undergoing lower abdominal surgeries receiving QL block with those receiving caudal bupivacaine/ neostigmine.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date April 30, 2021
Est. primary completion date April 30, 2021
Accepts healthy volunteers No
Gender All
Age group N/A to 15 Years
Eligibility Inclusion Criteria: - Patients American Society of Anesthesiologists physical status (ASA) I or II. - Consent from parents or legal guardian(s). - Lower abdominal surgeries. Exclusion Criteria: - Parents' refusal or legal guardian's refusal. - Infection at the injection site. - Known allergy to bupivacaine and/or neostigmine. - Contraindications to regional anesthesia (including coagulopathy and local infection). - Anatomical anomalies at the site of the block.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
bupivacaine/ neostigmine.
will receive bilateral ultrasound guided QLB
bupivacaine/ neostigmine.
will receive ultrasound guided CB.

Locations

Country Name City State
Egypt Ain-Shams University Hospitals Cairo

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary The total amount of paracetamol doses (mg) The total amount of paracetamol doses (mg) 24 hours postoperatively
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