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NCT06705595
The Effect of Local Anesthetic Techniques on Hemodynamic Response and Postoperative Sore Throat in Double-Lumen Tubes
NA trial testing Tracheo-Spray in Anesthesia, Local in 60 participants. Completed in 12 December 2024.
6 December 2024
Quick facts
| Lead sponsor | V.K.V. American Hospital, Istanbul |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | prevention |
| Enrollment | 60 |
| Start date | 6 November 2024 |
| Primary completion | 6 December 2024 |
| Estimated completion | 12 December 2024 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- Tracheo-Spray — full drug profile →
- Lidocaine Spray on DLT — full drug profile →
- Saline (Placebo)
Conditions studied
- Anesthesia, Local — all drugs for Anesthesia, Local →
- Intubation, Intratracheal — all drugs for Intubation, Intratracheal →
- Double-lumen Tube — all drugs for Double-lumen Tube →
- Sore Throat — all drugs for Sore Throat →
Sponsor
V.K.V. American Hospital, Istanbul
Who can join
18 and older, any sex, with Anesthesia, Local or Intubation, Intratracheal. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This clinical trial aims to determine if different local anesthetic application techniques can reduce postoperative sore throat (POST) and manage hemodynamic responses in adult patients undergoing elective thoracic surgery with double-lumen intubation. The main questions it aims to answer are: * Does inhaled lidocaine or lidocaine applied to the double-lumen tube reduce the incidence and severity of POST? * How do these anesthetic techniques impact hemodynamic stability during surgery? Researchers will compare three groups-those receiving inhaled lidocaine, lidocaine applied to the tube, and a saline control group-to see if these methods differ in effectiveness. Participants will: * Undergo standard preoperative assessment and provide informed consent * Be randomly assigned to receive either inhaled lidocaine, lidocaine applied to the tube, or saline * Have sore throat scores and hemodynamic data recorded at specific intervals after surgery
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT06705595
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other V.K.V. American Hospital, Istanbul trials
Trials by the same sponsor.
- NCT06707818 — Psychosocial Factors and Postoperative Pain in Aesthetic Breast Surgery · completed
- NCT06138119 — The Impact of Gender Stereotypes on Fiberoptic Intubation Performance · NA · completed
- NCT05242198 — Rectus Sheath Block May Relieve Urethral Catheter Pain · NA · completed
- NCT05241977 — MINIMUM EFFECTIVE VOLUME OF BUPIVACAİNE FOR ANTERIOR SUPRASCAPULAR NERVE BLOCK · completed
- NCT05282303 — REGIONAL ANALGESIA TECHNIQUES FOR EFFECTIVE RECOVERY TO CORONARY ARTERY BYPASS SURGERIES: A RETROSPECTİVE STUDY IN A SIN · completed
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 NCT06705595 (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 V.K.V. American Hospital, Istanbul
- Last refreshed: 13 January 2025
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/NCT06705595.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing