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Combined PECS II and Transeversus Thoracic Plane Blocks Vs Serratus Anterior Plane Block in Modified Radical Mastectomy

Analgesic Efficacy of Combined Ultrasound-Guided PECS II and Transeversus Thoracic Plane Blocks Versus Ultrasound-Guided Serratus Anterior Plane Block in Modified Radical Mastectomy: A Prospective Randomized Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04908878
Enrollment
70
Registered
2021-06-01
Start date
2021-06-01
Completion date
2022-06-02
Last updated
2022-11-29

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

Conditions

Modified Radical Mastectomy, Pectoral Nerve (PECS) Block, Serratus Anterior Plane Block, Transeversus Thoracic Plane Blocks, Ultrasound-Guided

Brief summary

The aim of this study is to evaluate the analgesic efficacy of combined ultrasound (US)-guided pectoral nerve (PECS) block II and transversus thoracic plane (TTP) block versus US-guided serratus anterior plane (SAP) block in female patients undergoing modified radical mastectomy.

Interventions

PROCEDUREPectoral nerve (PECS) block -transversus thoracic plane (TTP) block

Patients will receive unilateral US-guided PECS II block and TTP block on the side of the operation after induction of general anesthesia.

Patients will receive US-guided SAP block after induction of general anesthesia.

Sponsors

Tanta University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
FEMALE
Age
21 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Female patients * Aged 21-60 years * ASA physical status I, II * Scheduled for unilateral modified radical mastectomy

Exclusion criteria

1. Patient refusal. 2. Known hypersensitivity to local anesthetics. 3. Body mass index \> 35 kg /m2. 4. Uncooperative or psychiatric patients. 5. Infection at the injection site. 6. Coagulation disorder.

Design outcomes

Primary

MeasureTime frameDescription
The total amount rescue analgesic consumption (morphine) in the first 24 hours postoperatively.First 24 hours postoperatively.Rescue analgesia in the form of morphine (3mg IV) will be given if the VAS is ≥ 40, repeated with lock out interval of 5 min guided with the occurrence of complications till the VAS is decreased to less than 40.

Secondary

MeasureTime frameDescription
The degree of postoperative painFirst 24 hours postoperatively.Postoperative pain will be assessed by Visual Analog scale (VAS) on admission to Post-Anesthesia Care unit (PACU) and at 30 minutes and then 1,2,4,6,12,18 and 24 hours postoperative. VAS (0-100; where 0 represents no pain and 100 represents the worst pain).
Time to first rescue analgesia request.First 24 hours postoperatively.Rescue analgesia in the form of morphine (3mg IV) will be given if the VAS is ≥ 40, repeated with lock out interval of 5 min guided with the occurrence of complications till the VAS is decreased to less than 40.
Intraoperative fentanyl consumption.IntraoperativeAdditional boluses of fentanyl 0.5 µg /kg will be administered in case of inadequate analgesia that defined as increase of heart rate (HR) and /or mean arterial blood pressure (MAP) more than 20 % from baseline

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026