Adding Calcitonin to Bupivacaine in Transversalis Fascia Plane Block for Cesarean Section
Analgesic Effect of Adding Calcitonin to Bupivacaine in Transversalis Fascia Plane Block for Cesarean Section, A Prospective Randomized Study
1 other identifier
interventional
70
1 country
1
Brief Summary
Evaluate calcitonin as an adjuvant to bupivacaine in ultrasound guided tansversalis fascia plane block
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 Apr 2025
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
Study Start
First participant enrolled
April 1, 2025
CompletedFirst Submitted
Initial submission to the registry
June 13, 2025
CompletedFirst Posted
Study publicly available on registry
June 24, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2025
CompletedJune 24, 2025
May 1, 2025
4 months
June 13, 2025
June 23, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
time to first rescue analgesia
24 hours
Study Arms (2)
Transversalis fascia plane block with bupivacaine
ACTIVE COMPARATORus guided transversalis fascia plane block with bupivacaine
Transversalis fascia plane block with calcitonin and bupivacaine
ACTIVE COMPARATORus guided transvesalis fascia plane block with calcitonin and bupivacaine
Interventions
addition of calcitonin to pubivacaine
Eligibility Criteria
You may qualify if:
- female pt ASA2 scheduled for cs under spinal anesthesia
You may not qualify if:
- patient refusal ASAmore than 3 patients with pregnancy related disease emergency cs history of coagulopathy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Tanta Universitylead
Study Sites (1)
tanta University hospital
Tanta, Gharbia Governorate, Egypt
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, CARE PROVIDER
- Purpose
- PREVENTION
- Intervention Model
- SEQUENTIAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Marwa Abogabal
Study Record Dates
First Submitted
June 13, 2025
First Posted
June 24, 2025
Study Start
April 1, 2025
Primary Completion
August 1, 2025
Study Completion
September 1, 2025
Last Updated
June 24, 2025
Record last verified: 2025-05