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Transversus Abdominis and Transversalis Fascia Plane Block Combination for Cesarean Section

Combined Transversalis Fascia and Transversus Abdominis Plane Blocks Versus Intrathecal Morphine: Effects on Postoperative Opioid Consumption and Obstetric Recovery After Cesarean Section

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06944912
Acronym
TAPTFPB
Enrollment
100
Registered
2025-04-25
Start date
2024-01-01
Completion date
2025-03-01
Last updated
2025-04-27

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

Conditions

Ceserean Section and Postoperative Pain

Keywords

Postoperative Recovery, Cesarean Section, Postoperative Pain, Transversalis Fascia Plane Block, Transversus Abdominis Plane Block, Intrathecal Opioid, ObsQoR-10 T

Brief summary

Cesarean delivery rates are rising globally, and effective postoperative analgesia is crucial for maternal recovery and newborn care. While intrathecal morphine offers strong analgesia, it may cause side effects such as nausea, pruritus, or respiratory depression. The transversus abdominis plane (TAP) block provides somatic pain relief but is often insufficient alone. The transversalis fascia plane block (TFPB) has been shown to enhance lower abdominal analgesia. This study aims to evaluate whether combining TAP and TFP blocks can provide analgesic efficacy comparable to intrathecal morphine in cesarean section patients who are unable to receive opioids or are at high risk of side effects.

Interventions

PROCEDURETransversalis fascia plane block and transversus abdominis plane block

20 ml local anesthetics for Transversus Abdominis Plane block and 10 ml local anesthetics for Trasnversalis fascia plane block

PROCEDUREIntrathecal Morphine

100 mcg morphine with local anesthetics injected intrathecally

Sponsors

Ataturk University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* 18-45 years old * American Society of Anesthesiologists physical score I or II * caesarean section with a Pfannenstiel incision

Exclusion criteria

* additional surgical intervention, or received general anaesthesia, * hypersensitivity to the agents to be used * BMI greater than 35 kg m-2 * coagulopathy, * local infection, * opioid addiction, * pregnancy-related hypertension * diabetes mellitus

Design outcomes

Primary

MeasureTime frameDescription
The Obstetric Quality of Recovery-10 (ObsQoR-10) ScorePostoperative 24 hoursThe questionnaire's subscales are physical comfort (n=3 items), emotional state (n=2 items), pain (n=1 item), physical independence (n=2 items), and the ability to take care of the newborn (n=2 items). Each item is scored on a scale of 0-10, except for the first four items, which are graduated from 10 to 0. The total score is the sum of all item scores (i.e. a score ranging from 0 to 100, where 0 is the worst recovery score, and 100 indicates the best).

Secondary

MeasureTime frameDescription
Opioid consumptionPostoperative 24. hoursPatient controlled analgesia based opioid requirement

Countries

Turkey (Türkiye)

Outcome results

None listed

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