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Effect of Propofol on Remifentanil-induced Postoperative Hyperalgesia in Patients Undergoing Thyroid Surgery

Y

Yonsei University Health System (YUHS)

Status and phase

Unknown
Phase 4

Conditions

Hyperalgesia

Treatments

Drug: propofol, sevoflurane

Study type

Interventional

Funder types

Other

Identifiers

NCT01189721
3-2010-0102

Details and patient eligibility

About

The investigators hypothesize that propofol infusion during surgery can affect the remifentanil hyperalgesia compared to sevoflurane inhalation.The outcome will be measured by a verbal numerical rating score (VNRS) and mechanical punctuating pain by electronic von frey filament.

Enrollment

84 estimated patients

Sex

All

Ages

20 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing thyroidectomy
  • Age 20-65
  • American Society of Anesthesiologists physical status classification I or II

Exclusion criteria

  • History of chronic pain, Regular use of analgesic, antiepileptic or antidepressive drugs
  • History of drug & alcohol abuse
  • Psychiatric disorder
  • Use of opioids within 24hrs
  • Renal disease with decreased glomerular filtrate ratio
  • Neuromuscular disease, Severe cardiac disease

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

84 participants in 2 patient groups

sevoflurane
Active Comparator group
Description:
Remifentanil will be infused intraoperatively at 0.2 ㎍/㎏/min. patients who are in this group will be infused propofol intraoperatively.
Treatment:
Drug: propofol, sevoflurane
propofol
Experimental group
Description:
Remifentanil will be infused intraoperatively at 0.2 ㎍/㎏/min. patients included this group will be inhaled sevoflurane intraoperatively.
Treatment:
Drug: propofol, sevoflurane

Trial contacts and locations

1

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Central trial contact

young ju won, MD.; yuen hee shim, MD.

Data sourced from clinicaltrials.gov

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