Optimizing Postoperative Pain Control After Laparoscopic Colorectal Surgery
NCT ID: NCT06007378
Last Updated: 2025-07-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
120 participants
INTERVENTIONAL
2023-09-05
2025-07-22
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
DOUBLE
Study Groups
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Bupivacaine and ketamine
Bupivacaine and ketamine
Bilateral erector spinae plane block (bupivacaine and ketamine)
Bupivacaine and transdermal fentanyl patch
Bupivacaine and transdermal fentanyl patch
Bilateral erector spinae plane block (bupivacaine) and transdermal fentanyl patch
Bupivacaine
Bupivacain
Bilateral erector spinae plane block (bupivacaine)
Interventions
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Bupivacaine and ketamine
Bilateral erector spinae plane block (bupivacaine and ketamine)
Bupivacaine and transdermal fentanyl patch
Bilateral erector spinae plane block (bupivacaine) and transdermal fentanyl patch
Bupivacain
Bilateral erector spinae plane block (bupivacaine)
Eligibility Criteria
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Inclusion Criteria
* American Society of Anesthesiologists (ASA) physical status I or II.
Exclusion Criteria
* Skin infections at the site of the needle puncture.
* Hepatic, renal or cardiac dysfunction.
* Patients diagnosed with obstructive sleep apnoea
21 Years
ALL
No
Sponsors
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Ain Shams University
OTHER
Responsible Party
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Ibrahim Mamdouh Esmat
Assistant Professor of Anesthesia and Intensive Care, Faculty of Medicine, Ain- shams University, Cairo, Egypt.
Locations
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Ain-Shams University Hospitals
Cairo, , Egypt
Countries
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Other Identifiers
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FMASU MS 416 / 2023
Identifier Type: -
Identifier Source: org_study_id
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