Ultrasound Guided TAPB vs Surgical TAPB With Bupivacaine in Cesarean Section

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age21-35
SponsorAl-Azhar University

About this trial

The aim of this study is to compare Surgical Transversus abdominis plane block and Ultrasound guided transversus abdominis plane block (TAPB) as a postoperative analgesic regimen in female patients undergoing elective cesarean delivery.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Full term pregnant women

Older than 21 years of age

Had elective cesarean section with Pfannenstiel incision.

Disqualifiers

Patients with cesarean section using different surgical incision

History of addiction [including opioids and benzodiazepines]

Allergy to the anesthetic analgesia

Psychological disorders

Trial design

Design model

Parallel

Treatments tested in this trial

  • surgical TAP block

    Procedure/Surgery

    performed by 40 ml of 0.25% bupivacaine (10 ml 0.5% bupivacaine bilaterally diluted with 10cc normal saline and 100 μg of fentanyl), the total volume was divided equally and administered bilaterally by the surgeon.

  • US guided TAP block

    Procedure/Surgery

    performed by 40 ml of 0.25% bupivacaine (10 ml 0.5% bupivacaine bilaterally diluted with 10cc normal saline and 100 μg of fentanyl), the total volume was divided equally and administered bilaterally.

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: surgical TAP blockActive comparator 1 intervention
Group B: US guided TAP blockActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Time to perform block.

The time taken to perform the block will be recorded by an independent observer.

Time frame
1 hour postoperatively

Secondary outcomes

1

Heart rate

Patients hemodynamics (heart rate will be recorded)

Time frame
24 hours postoperatively
2

Mean arterial blood pressure

Patients hemodynamics (mean arterial blood pressure will be recorded)

Time frame
24 hours postoperatively
3

Pain score

The Visual Analogue Scale (VAS) measures pain intensity. The VAS consists of a 10cm line, with two end points representing 0 ('no pain') and 10 ('pain as bad as it could possibly be').

Time frame
24 hours postoperatively
4

Time to first analgesic request

The time to first analgesic request will be recorded

Time frame
24 hours postoperatively

Other outcomes

Sponsors and contacts

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