Erector Spinae Plane Block Versus Lateral Transversus Abdominis Plane Block for Open Abendectomy Surgery
Analgeisc Effect of Erector Spinae Plane Block Versus Lateral Transversus Abdominis Plane Block in Patients Undergoing Open Abendectomy Surgery: a Randomized Controlled Trial
1 other identifier
interventional
68
1 country
1
Brief Summary
this aim of this study is to compare the analgesic effect of Erector spinae plane (ESP) block and lateral transversus abdominis plan (TAP) block in patients undergoing open appendectomy.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jan 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 10, 2026
CompletedFirst Posted
Study publicly available on registry
January 20, 2026
CompletedStudy Start
First participant enrolled
January 25, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
May 1, 2026
March 17, 2026
January 1, 2026
3 months
January 10, 2026
March 15, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Total morphine consumption
mg
from extubation until 24 hours postoperative
Secondary Outcomes (2)
numeric rating scale
AT 0.5, 2, 6, 12, and 24 hours postoperative.
quality of recovery
24 hours after suregry
Study Arms (2)
ESP group
ACTIVE COMPARATORTAP group
ACTIVE COMPARATORInterventions
Patients will receive the ESP block at the level of the 10th thoracic (T10) transverse process using a linear 6-13 MHz ultrasound transducer. A 20 mL of 0.25% bupivacaine will be injected below the muscle
Patient will received TAP block using the lateral approach while in supine position. A 20 mL of 0.25% bupivacaine will be injected after negative aspiration.
Eligibility Criteria
You may qualify if:
- adult patients, undergoing open appendectomy.
You may not qualify if:
- American society of anesthesiologist-physical status \>III,
- allergy to any of the study drugs,
- coagulopathy
- local infection,
- history of chronic pain or regular opioid use;
- inability to comprehend the Numeric Rating Scale (NRS),
- pregnant or lactating women.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (1)
Cairo University
Cairo, Cairo Governorate, Egypt
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
January 10, 2026
First Posted
January 20, 2026
Study Start
January 25, 2026
Primary Completion (Estimated)
May 1, 2026
Study Completion (Estimated)
May 1, 2026
Last Updated
March 17, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will not share
data regarding this research will be available upon reasonable request from the PI