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NCT03571867
Comparison of The Severity of Agitation of Sugammadex and Atropine-Nesostigmine in Adenotonsillectomy
trial in The Severity of Agitation in Adenotonsillectomy in Pediatric Patients in 70 participants. Status unknown.
1 September 2018
Quick facts
| Lead sponsor | Sakarya University |
|---|---|
| Status | Status unknown |
| Study type | OBSERVATIONAL |
| Enrollment | 70 |
| Start date | 1 July 2018 |
| Primary completion | 1 September 2018 |
| Estimated completion | 1 November 2018 |
| Sites | 1 location across Turkey (Türkiye) |
Conditions studied
- The Severity of Agitation in Adenotonsillectomy in Pediatric Patients — all drugs for The Severity of Agitation in Adenotonsillectomy in Pediatric Patients →
Sponsor
Sakarya University
Who can join
Adults 5 to 13, any sex, with The Severity of Agitation in Adenotonsillectomy in Pediatric Patients. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
the use of sugammadex during the reversal of neuromuscular blocking after adenotonsillectomy surgery in pediatric patients would be advantageous in terms of patient comfort and reducing side effects. Thus, we aimed to evaluate the time to extubation, agitation and pain scores in pediatric patients who underwent adenotonsillectomy and awakened with neostigmine and sugammadex in our study.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
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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 NCT03571867 (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 Sakarya University
- Last refreshed: 28 June 2018
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/NCT03571867.
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