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NCT05255536
Effect of Different Local Anesthetic Volumes of Serratus Anterior Plan Block After Video-Assisted Thoracoscopic Surgery
NA trial testing Serratus Anterior Plan Block with 20 ml in Serratus Anterior Plane Block in 60 participants. Status unknown.
15 April 2024
Quick facts
| Lead sponsor | Atatürk Chest Diseases and Chest Surgery Training and Research Hospital |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 60 |
| Start date | 15 February 2022 |
| Primary completion | 15 April 2024 |
| Estimated completion | 15 May 2024 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- Serratus Anterior Plan Block with 20 ml
- Serratus Anterior Plan Block with 30 ml
Conditions studied
- Serratus Anterior Plane Block — all drugs for Serratus Anterior Plane Block →
- Pain, Postoperative — all drugs for Pain, Postoperative →
- Thoracic Surgery, Video-Assisted — all drugs for Thoracic Surgery, Video-Assisted →
- Local Anesthetic — all drugs for Local Anesthetic →
Sponsor
Atatürk Chest Diseases and Chest Surgery Training and Research Hospital
Who can join
Adults 18 to 65, any sex, with Serratus Anterior Plane Block or Pain, Postoperative. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
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.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT05255536
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Currently open trials in the same condition.
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Other Atatürk Chest Diseases and Chest Surgery Training and Research Hospital trials
Trials by the same sponsor.
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- NCT06338007 — Relationship Between Hand Dynamometer Measurements, PFT, and mFI With Postoperative Outcomes · not yet recruiting
- NCT06341933 — Risk Factors for AKI in Patients Undergoing VATS for Pulmonary Resection · recruiting
- NCT06303557 — Effect of ESPB on Intraoperative Remifentanil Consumption · NA · completed
- NCT06247631 — STOP-Bang Questionnaire: A Predictor of Obstructive Sleep Apnea and Difficult Mask/Intubation? · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05255536 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Atatürk Chest Diseases and Chest Surgery Training and Research Hospital
- Last refreshed: 2 February 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05255536.
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