Clinical Trials Directory

Trials / Completed

CompletedNCT04054479

Penehyclidine for PONV Prophylaxis After Strabismus Surgery

The Effect of Penehyclidine on Postoperative Nausea and Vomiting After Strabismus Surgery

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
228 (actual)
Sponsor
The First Affiliated Hospital with Nanjing Medical University · Academic / Other
Sex
All
Age
3 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Patients scheduled for elective strabismus surgery under general anesthesia in the First Affiliated Hospital of Nanjing Medical University will be included in this study. Patients 1)ASA I or II, 2)aged 3-65 years, 3)scheduled for elective strabismus surgery under general anesthesia, will be included in the study. Patients 1)had prior PONV, 2)severe motion sickness, 3)a history of ophthalmic surgery, 4)had received drugs known to have antiemetic effects, will be excluded from the study. The primary aim is to evaluate the prophylaxis effect of penehyclidine(a novel long acting selective anticholinergic agent developed in China) on postoperative nausea and vomiting after strabismus surgery. Secondary outcomes include the effect of PONV risk factors and surgical technique on PONV rank score, occurance of oculocardiac reflex, time to extubation.

Conditions

Interventions

TypeNameDescription
DRUGPenehyclidinePatients receive penehyclidine 10μg/kg(up to 0.5mg, diluted with normal saline to 0.1mg/ml) after anesthesia intubation.
DRUGnormal salinePatients receive 0.1ml/kg normal saline(up to 5ml) after anesthesia intubation.

Timeline

Start date
2019-07-20
Primary completion
2019-07-22
Completion
2019-11-01
First posted
2019-08-13
Last updated
2019-12-17

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04054479. Inclusion in this directory is not an endorsement.