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NCT03515694
Minimal Optimal Dose of Sugammadex in Elective Surgery
Phase 4 trial testing Sugammadex Injection [Bridion] in Time of a TOF Ratio >0,9 in 40 participants. Completed in 30 September 2018.
30 September 2018
Quick facts
| Lead sponsor | Erasme University Hospital |
|---|---|
| Phase | Phase 4 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 40 |
| Start date | 3 April 2018 |
| Primary completion | 30 September 2018 |
| Estimated completion | 30 September 2018 |
| Sites | 1 location across Belgium |
Drugs / interventions tested
- Sugammadex Injection [Bridion] — full drug profile →
Conditions studied
- Time of a TOF Ratio >0,9 — all drugs for Time of a TOF Ratio >0,9 →
Sponsor
Erasme University Hospital
Who can join
18 and older, any sex, with Time of a TOF Ratio >0,9. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Time of appearance of TOF Ratio \>0,9 with different doses of Sugammadex
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 NCT03515694
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Sugammadex Injection [Bridion]
Trials testing the same drug.
- NCT03087513 — A Randomized Controlled Crossover Study Comparing Sugammadex and Placebo · Phase 4 · completed
- NCT03229486 — Effect of Sugammadex vs. Neostigmine/Glycopyrrolate on Pediatric Emergence Delirium in Sevoflurane-rocuronium Anesthesia · Phase 4 · completed
Other Erasme University Hospital trials
Trials by the same sponsor.
- NCT07532733 — Respiratory and Haemodynamic Effects of Conscious Sedation With Dexmedetomidine for a TAVI Procedure · NA · not yet recruiting
- NCT07532681 — Effect of Early Versus Late Surgical Intercostal Block on Postoperative Pain Relief Following Video-Assisted Thoracic Su · NA · not yet recruiting
- NCT07457879 — Impact of the Reimbursement of Fibrinogen in Cardiac Surgery · not yet recruiting
- NCT07184593 — Nucleosome Monitoring Relevance for Outcome Prediction in Critically Ill Patients · not yet recruiting
- NCT07369232 — Cerebral Hemodynamic Effects of Oxygen and Antioxidants (CHEOXANT) · NA · 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 NCT03515694 (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 Erasme University Hospital
- Last refreshed: 15 February 2019
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/NCT03515694.
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