Actively Recruiting
Efficacy of Trans Abdominis Plane Block for Post Cesarean Delivery Analgesia
Led by Qassim University · Updated on 2024-08-16
100
Participants Needed
1
Research Sites
21 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Relief from pain is part of the fundamental human right to health. (1) However, available evidence indicates an increasingly detailed understanding of the pathophysiology of pain and general inadequacy of its treatment.
CONDITIONS
Official Title
Efficacy of Trans Abdominis Plane Block for Post Cesarean Delivery Analgesia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 20 and 50 years
- Weight between 50 kg and 100 kg
- Scheduled for elective, emergent, or urgent cesarean section
You will not qualify if you...
- Weight less than 50 kg or greater than 100 kg
- Any contraindication to anesthesia medications
- Unable to understand the numeric rating scale for pain assessment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Qassim University Medical City
Buraidah, Al-Qassim Region, Saudi Arabia, 51411
Actively Recruiting
Research Team
H
HANI ALNAJJAR, BSN
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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