Last reviewed · How we verify
NCT06592027: Precedex
Dexmedetomidine for Attenuation of Pressor Response
Phase 4 trial testing PRECEDEX INJ★ 2ML in Pressor Response in 60 participants. Completed in 30 May 2024.
1 May 2024
Quick facts
| Lead sponsor | Theodor Bilharz Research Institute |
|---|---|
| Phase | Phase 4 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | quadruple |
| Primary purpose | treatment |
| Enrollment | 60 |
| Start date | 1 February 2024 |
| Primary completion | 1 May 2024 |
| Estimated completion | 30 May 2024 |
| Sites | 1 location across Egypt |
Drugs / interventions tested
- PRECEDEX INJ★ 2ML — full drug profile →
- PRECEDEX INJ★ 2ML — full drug profile →
Conditions studied
- Pressor Response — all drugs for Pressor Response →
Sponsor
Theodor Bilharz Research Institute
Who can join
Adults 18 to 60, any sex, with Pressor Response. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Direct laryngoscopy and tracheal intubation are usually associated by hemodynamic changes due to increased sympathoadrenal activity which could precipitate serious negative effects in compromised patients . The pressor response could be blunted by dexmedetomidine which is a selective alpha 2 agonist which might provide hemodynamic stability during tracheal intubation.
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 NCT06592027
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of PRECEDEX INJ★ 2ML
Trials testing the same drug.
- NCT06176222 — Combined Use of Naldebain® ER Injection and Precedex® After VATS · Phase 4 · unknown
Other Theodor Bilharz Research Institute trials
Trials by the same sponsor.
- NCT06872138 — S100A8 in Serum and Urine as a New Biomarker in Lupus Nephritis · completed
- NCT07262398 — Unilateral Intrathecal Bupivacaine Versus Prilocaine on Postoperative Spontaneous Voiding · Phase 4 · completed
- NCT06414395 — The Effects of Different Loading Doses of Dexmedetomidine on The Bispectral Index-Guided Propofol Sedation in Patients U · Phase 4 · recruiting
- NCT06541613 — Bilateral External Oblique Intercostal Plane Block in Laparoscopic Cholecystectomy · Phase 4 · completed
- NCT07481812 — Prolapsed Hemorrhoids: Assessment of Various Surgical Modalities · NA · 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 NCT06592027 (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 Theodor Bilharz Research Institute
- Last refreshed: 19 September 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/NCT06592027.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing