ClinicalTrials.Veeva

Menu

Effect of Daytime Variation on Postoperative Hyperalgesia Induced by Opioids

C

Chongqing Medical University

Status

Completed

Conditions

Postoperative Hyperalgesia

Treatments

Drug: Remifentanil

Study type

Observational

Funder types

Other

Identifiers

NCT05234697
Postoperative hyperalgesia

Details and patient eligibility

About

To explore the effect of daytime variation on postoperative hyperalgesia induced by opioids. Patients receiving endoscopy surgery under general anesthesia during 08:00-12:00(morning group, n=30) and 14:00-18:00(afternoon group, n=30) using remifentanil for anesthesia maintenance were respectively included. Postoperative hyperalgesia at PACU and 24 hours after surgery were assessed through mechanical pain measurement. Comparative analysis of postoperative hyperalgesia levels, pain and analgesic requirements between morning group and afternoon group were performed.

Enrollment

60 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • American Society of Anesthesiologists classification I-II
  • Abdominal endoscopy surgery
  • Estimated surgery duration 1-2h
  • Right handedness
  • Voluntarily receive postoperative intravenous controlled analgesia

Exclusion criteria

  • Heavy smoking or alcohol dependence
  • Puerpera or lactation women
  • History of chronic pain
  • Analgesic use within one month before surgery
  • Allergy to opioids
  • Can not follow with the study procedure

Trial design

60 participants in 2 patient groups

Morning group
Description:
Surgery performed during 08:00 to 12:00
Treatment:
Drug: Remifentanil
Afternoon group
Description:
Surgery performed during 14:00 to 18:00
Treatment:
Drug: Remifentanil

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems