Clinical Trials Directory

Trials / Completed

CompletedNCT04396587

Non-analgesic Effects Produced by Equipotent Analgesic Doses of Sufentanil, Hydromorphone, and Oxycodone

Non-analgesic Effects Produced by Equipotent Analgesic Doses of Sufentanil, Hydromorphone, and Oxycodone in Female Patients Before Anesthesia Induction

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
80 (actual)
Sponsor
Peking University People's Hospital · Academic / Other
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Not accepted

Summary

This study aimed to investigate Non-analgesic Effects Produced by Equipotent Analgesic Doses of Sufentanil, Hydromorphone, and Oxycodone in female patients. Methods: A total of 60 patients were randomly divided into 4 groups, with 20 patients in each group. Sufentanil(0.1μg/kg), Hydromorphone(20μg/kg), or Oxycodone(60μg/kg) ,saline(10ml)was administered before anesthesia induction. Bispectral Index (BIS), Respiratory rate(RR), other non-analgesic effects at Tb (entering room), T0 (drug administration), T1 (2min), T2 (4min), T3(6min), T4(8min), T5(10min), T6(20min) were recorded.

Conditions

Interventions

TypeNameDescription
DRUGSufentanilSufentanil(0.1μg/kg) was administered before anesthesia induction.
DRUGHydromorphoneHydromorphone(20μg/kg)was administered before anesthesia induction.
DRUGOxycodoneOxycodone(60μg/kg) was administered before anesthesia induction.
DRUGnormal Salinenormal saline 10ml

Timeline

Start date
2020-05-20
Primary completion
2023-01-01
Completion
2023-06-01
First posted
2020-05-20
Last updated
2024-05-30

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04396587. Inclusion in this directory is not an endorsement.