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Transversus Abdominis Plane Block for Post-operative Analgesia Following Cesarean Section

Transversus Abdominis Plane Block: Ultra-sound Guided Versus the Modified Surgeon Assisted Approaches for Post-operative Analgesia Following Cesarean Section

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05136118
Enrollment
308
Registered
2021-11-29
Start date
2021-11-01
Completion date
2022-10-25
Last updated
2022-10-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Analgesia

Keywords

post-operative analgesia, Transversus Abdominis Plane Block

Brief summary

Postpartum analgesia is a common concern after Cesarean Section (CS). The quality of postoperative recovery is improved by opioid sparing pain control approaches. The transversus abdominis plane block (TAPB) is an effective technique for postpartum analgesia after cesarean section. Pregnancy results in thinning of the internal oblique aponeurosis; with increased incidence of missing the second pop to reach the transversus abdominis plane (TAP). The classic blind approach to the TAP is associated with several complications; so, it has been largely replaced by the ultrasound-guided approach to the TAP. The ultrasound-guided approach to the TAPB was first described by Hebbart and his colleagues in 2007.Ultrasound-guided TAPB improves the success of the block, reduces the volume of local anesthetic used and prevents the potential injury of adjacent structures. Surgical approach to the TAPB was also described, it is a quick and easy approach of establishing a reliable block. The surgeon performs an intra-abdominal approach to the TAPB; by which asepsis is easily attained, visible and tactile confirmation of correct needle placement may be achieved with no risk of damage to the viscera but care must be given to avoid injury of the inferior epigastric vessels.

Detailed description

Compare the Transversus Abdominis Plane Block via the modified surgeon assisted approach (Study group), to the ultra-sound guided approach (Control group); as regards the post-operative analgesia following Cesarean Section.

Interventions

PROCEDURETAPB

TAPB will be given to parturients whether by the modified surgeon assisted approach or by the ultra-sound guided approach.

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
21 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* ASA physical status I and ∏ * primigravidas * aged 21-40 years * BMI ˂ 40 * body weight ˃ 60 kg * singleton pregnancy * gestational age of ≥37 weeks * undergoing elective caesarean section under spinal anesthesia.

Exclusion criteria

* Parturient refusal * parturient with a BMI \> 40 * body weight \< 60 kg * ASA physical status ≥ III * known local anesthetic (LA) allergy •contraindications to spinal anesthesia * parturients who received analgesics in the past 24 hours * infection at the site of the block.

Design outcomes

Primary

MeasureTime frameDescription
Time to rescue analgesia6 monthsthe time from the end of surgery until the first parturient's request for analgesia

Secondary

MeasureTime frameDescription
Efficacy of the modified surgeon assisted approach for TAPB on postoperative analgesia6 monthsassessment of pain intensity at rest and on passive flexion of the hip and knee by the Numeric Pain Rating Score (NPRS) from 0 = no pain to 10 = worst pain. Assessment will be done at 2, 6, 12 and 24h postoperative.
Number of parturients requiring postoperative analgesia6 monthsdefined as pethidine needed by each parturient in the 24 hours postoperative period
Total dose of pethidine given6 monthsdefined as pethidine needed by each parturient in the 24 hours postoperative period
Time to the parturient's first ambulation6 monthsthe time to start of each parturient movement in the 24 hours postoperative period
The analgesic satisfaction 24 hours after operation6 monthsparturients will be asked to report their satisfaction with pain management, assessed as 0 = weak, 1 = medium, 2 = good, 3 = very good, and 4 = excellent.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026