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NCT04697836
Cervical Plexus Block Combined With Translaryngeal Block for Tracheostomy
NA trial testing ST in Regional Anesthesia Morbidity in 29 participants. Completed in 25 November 2020.
25 November 2020
Quick facts
| Lead sponsor | Namik Kemal University |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | supportive care |
| Enrollment | 29 |
| Start date | 1 March 2020 |
| Primary completion | 25 November 2020 |
| Estimated completion | 25 November 2020 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- ST
Conditions studied
- Regional Anesthesia Morbidity — all drugs for Regional Anesthesia Morbidity →
Sponsor
Namik Kemal University
Who can join
Adults 18 to 65, any sex, with Regional Anesthesia Morbidity. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Current healthcare delivery models emphasize enhanced postoperative recovery (ERAS) with minimal morbidity and shorter hospital stays. Most tracheostomy cases are tumour patients. The more the patients have difficulty in breathing, the more difficult it is to anaesthetize them. Adequate intraoperative anaesthesia and postoperative analgesia with minimal sedation play an essential role in this patient model. In tracheostomy patients, moving away from the general anaesthesia option increases airway safety, and avoiding the local anaesthesia option in the incision area increases patient comfort. The purpose of this study is to assess the safety and efficacy of regional anaesthesia in tracheostomy patients.
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 NCT04697836
- Europe PMC full search
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- ESMO Meeting Library
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Other recruiting trials for Regional Anesthesia Morbidity
Currently open trials in the same condition.
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- NCT06520150 — Evaluation of the Effectiveness of Two Methods of Regional Anesthesia During S-ICD Implantation Procedure. · NA · recruiting
- NCT06168903 — EOI Block Versus ESP Block in Laparoscopic Bariatric Surgery · NA · recruiting
- NCT05233462 — Height Adjusted Versus Standardized Dose of Bupivacaine for Spinal Anesthesia · NA · recruiting
Other Namik Kemal University trials
Trials by the same sponsor.
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- NCT07467304 — Nursing Education Provided After Cesarean Section Surgery. · NA · enrolling by invitation
- NCT05671484 — TFPB vs QLB III in Infra-umbilical Pediatric Surgeries · NA · completed
- NCT05928845 — Sternocleidomastoid Thickness in Sarcopenia · not yet 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 NCT04697836 (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 Namik Kemal University
- Last refreshed: 6 January 2021
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/NCT04697836.
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