Actively Recruiting

Phase Not Applicable
FEMALE
NCT07033104

Adding Calcitonin to Bupivacaine in Transversalis Fascia Plane Block for Cesarean Section

Led by Tanta University · Updated on 2025-06-24

70

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Evaluate calcitonin as an adjuvant to bupivacaine in ultrasound guided tansversalis fascia plane block

CONDITIONS

Official Title

Adding Calcitonin to Bupivacaine in Transversalis Fascia Plane Block for Cesarean Section

Who Can Participate

FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Female patient with ASA physical status 2 scheduled for cesarean section under spinal anesthesia
Not Eligible

You will not qualify if you...

  • Patient refusal
  • ASA physical status higher than 3
  • Patients with pregnancy-related diseases
  • Emergency cesarean section
  • History of blood clotting disorders (coagulopathy)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
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Trial Site Locations

Total: 1 location

1

tanta University hospital

Tanta, Gharbia Governorate, Egypt

Actively Recruiting

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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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Adding Calcitonin to Bupivacaine in Transversalis Fascia Plane Block for Cesarean Section | DecenTrialz