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Subarachnoid Block With Ultrasound-Guided Transversalis Fascia Plane Block for Cesarean Section

Subarachnoid Block With Ultrasound-Guided Transversalis Fascia Plane Block for Cesarean Sections: A Randomized Placebo-Controlled Double-Blind Study

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04172727
Enrollment
60
Registered
2019-11-21
Start date
2019-01-01
Completion date
2019-06-01
Last updated
2019-11-21

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

Conditions

Caesarean Section, Pain, Acute

Brief summary

Postoperative pain management is critical for the fulfillment of the maternal duties. The transversalis fascia plane (TFP) block provides adequate postoperative analgesia in the T12 and L1 dermatomes. The aim of this study was to investigate the effect of the TFP block on postoperative opioid consumption and pain scores in patients undergoing cesarean section (CS) under spinal anesthesia.

Interventions

ultrasound-guided bilateral TFP block with 20 mL of 0.25% bupivacaine

DRUGsaline 0.9%

ultrasound-guided bilateral TFP block with 20 mL of saline 0.9%

Sponsors

Ataturk University
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* aged between 18 and 45 * American Society of Anesthesiologists (ASA) physical score I or II

Exclusion criteria

* Patients who received general anesthesia * hypersensitivity to the agents to be used * body mass index (BMI) greater than 35 kg/m2 * coagulopathy * local infections * opioid addiction * pregnancy-related hypertension or diabetes mellitus

Design outcomes

Primary

MeasureTime frameDescription
opioid consumptionPostoperative first 24hourmorphine consumption first 24hour

Secondary

MeasureTime frameDescription
pain scorespostoperative 0-24 hoursVisual Analogue Scale (0-10)

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026