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Effect of Different Local Anesthetic Volumes of Serratus Anterior Plan Block After Video-Assisted Thoracoscopic Surgery

The Effect of Different Local Anesthetic Volumes of Serratus Anterior Plan Block Performed With Ultrasound on Acute Pain After Video-Assisted Thoracoscopic Surgery

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05255536
Enrollment
60
Registered
2022-02-24
Start date
2022-02-15
Completion date
2024-05-15
Last updated
2024-02-02

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

Conditions

Local Anesthetic, Pain, Postoperative, Serratus Anterior Plane Block, Thoracic Surgery, Video-Assisted

Brief summary

Video-assisted thoracic surgery (VATS) has become a common procedure in thoracic surgery. Severe postoperative pain may be encountered in patients undergoing VATS. Analgesic methods such as thoracic paravertebral block (TPVB), intercostal block, serratus anterior plane block (SAPB), and erector spinae plane block (ESPB) are widely used for VATS. Among these methods, ultrasound (US) guided TPVB is the most preferred method. In recent years, the frequency of application of plane blocks as a component of multimodal analgesia has been increased. ESPB and SAPB are some of them. In addition, SAPB application is increasing in patients who underwent thoracotomy and VATS. There is no consensus on the dose of analgesia in these studies. There are studies on volumes between 10 ml and 40 ml in the literature. In this study, it was aimed to compare the volumes of 20 ml and 30 ml containing local anesthetic at the same concentration (0.25% bupivacaine) of SAPB block to be performed with USG in patients who underwent VATS.

Interventions

PROCEDURESerratus Anterior Plan Block with 20 ml

Superficial serratus anterior plane block with 20 ml will be applied to the patients under real-time ultrasound guidance.

PROCEDURESerratus Anterior Plan Block with 30 ml

Superficial serratus anterior plane block with 30 ml will be applied to the patients under real-time ultrasound guidance.

Sponsors

Atatürk Chest Diseases and Chest Surgery Training and Research Hospital
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* 18 to 65 years old * ASA physical status I-II-III * BMI 18 to 30 kg/m2 * Elective video assisted thoracoscopic surgery

Exclusion criteria

* Patient refusing the procedure * Emergency surgery * Chronic opioid or analgesic use

Design outcomes

Primary

MeasureTime frameDescription
Pain Scores48 hours after surgeryPain will be assessed at rest and while coughing using the visual analog scale on a scale from 0 (no pain) to 10 (worst pain). Pain assessment will be done at 1st, 2nd, 4th, 8th, 16th, 24th and 48th hours after surgery.

Secondary

MeasureTime frameDescription
Morphine Consumption24 hours after surgeryMorphine consumption for 24 hours will be recorded

Countries

Turkey (Türkiye)

Contacts

Primary ContactMusa Zengin, MD
musazengin@gmail.com903125677233
Backup ContactAli Alagoz, Assoc Prof
mdalagoz@gmail.com+903125677232

Outcome results

None listed

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