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New treatment option for This Study Evaluates the Effects of Different Fascial Plane Blocks on...
Official title Comparison of SPSIP Block and SAP Block in Non-Intubated Uniportal VATS.
ClinicalTrials.gov ID: NCT07440199
What this study is testing
- What it's testing
- Comparison of Serratus Posterior Superior Intercostal Plane Block and Serratus Anterior Plane Block in Uniportal Video-Assisted Thoracoscopic Surgery Without Intubation Single-port video-assisted thoracoscopic surgery without intubation (NI-UniVATS) is a technique in which video-assisted thoracoscopic surgery is performed through a single port without intubating the patient. It differs significantly from traditional VATS.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 65
You may be able to join if
- The study included patients who:
- were aged 18-65 years,
- had an American Society of Anaesthesiologists (ASA) physical status classification of I-III,
- had a body mass index (BMI) \< 35 kg/m²,
- read and signed the informed consent form.
You likely can't join if
- Patients;
- Unable to communicate in Turkish or refusing to participate in the study,
- Unable to use the numerical pain rating scale (NRS),
- History of allergy to local anaesthetics or analgesics used in the study,
- Pregnant or breastfeeding,
- History of uncontrolled anxiety disorder or substance dependence,
See the full eligibility criteria
- The study included patients who:
- were aged 18-65 years,
- had an American Society of Anaesthesiologists (ASA) physical status classification of I-III,
- had a body mass index (BMI) \< 35 kg/m²,
- read and signed the informed consent form.
- Patients;
- Unable to communicate in Turkish or refusing to participate in the study,
- Unable to use the numerical pain rating scale (NRS),
- History of allergy to local anaesthetics or analgesics used in the study,
- Pregnant or breastfeeding,
- History of uncontrolled anxiety disorder or substance dependence,
- Previous thoracic surgery or history of thoracic trauma,
- Widespread pleural adhesions detected during preoperative assessment,
- Neuromuscular or peripheral nervous system disease,
- Diabetes mellitus, hepatic or renal insufficiency, or coagulation disorder,
- Chronic opioid or steroid use,
- Widespread pain syndrome,
- Receiving anticoagulant therapy,
- Patients with infection detected in the area where the block will be applied were excluded.
The study team makes the final eligibility decision.
Where it's taking place
- Elâzığ, Turkey (Türkiye)
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 65 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Elâzığ, Turkey (Türkiye). Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.