Actively Recruiting
Analgesic Effect of Adding Calcitonin to Bupivacaine in Transversalis Fascia Plane Block for Cesarean Section, A Prospective Randomized Study
Led by Tanta University · Updated on 2025-06-24
70
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate the effect of adding calcitonin to bupivacaine during an ultrasound-guided transversalis fascia plane block for women undergoing cesarean section. The study is a prospective randomized trial designed to compare pain relief methods in this surgical setting.
CONDITIONS
Brief Title
Adding Calcitonin to Bupivacaine in Transversalis Fascia Plane Block for Cesarean Section
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female patient classified as ASA II
- Scheduled for cesarean section under spinal anesthesia
You will not qualify if you...
- Patient refusal
- More than three patients with pregnancy-related disease
- Emergency cesarean section
- History of coagulopathy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single day during cesarean section
Participants receive a transversalis fascia plane block with either bupivacaine alone or with calcitonin added during cesarean section under spinal anesthesia.
1 treatment visit (in-person)
Duration - 24 hours after treatment
Participants are monitored for pain relief and time to first rescue analgesia for 24 hours after the block.
Approximately 1 follow-up visit or monitoring period
Trial Site Locations
Total: 1 location
1
tanta University hospital
Tanta, Gharbia Governorate, Egypt
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
SEQUENTIAL
Primary Purpose
PREVENTION
Number of Arms
2
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