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The Effect of Dexmedetomidine in the Management of Pain After Uterine Artery Embolization

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01578174
Enrollment
66
Registered
2012-04-16
Start date
2012-04-30
Completion date
2012-09-30
Last updated
2018-01-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain Control

Brief summary

The investigators examined the effect of dexmedetomidine in the management of pain after uterine artery embolization.

Detailed description

Leiomyoma are the most common female reproductive tract tumors. Uterine artery embolization(UAE) is a minimally invasive treatment alternative to hysterectomy and myomectomy. However, post-procedural pain control after UAE remains a major problem. Therefore, the aim of study is to evaluate the efficacy of dexmedetomidine in pain control after UAE.

Interventions

DRUGDexmedetomidine

Dexmedetomidine(Dexmedetomidine 2 mL and normal saline 98 mL mixed -\> 2㎍/mL) : the infusion of 0.2㎍/kg/hr is started at 30 minutes before the procedure and the infusion dose is raised to 0.4㎍/kg/hr after completion of procedure

DRUGNormal saline 0.9%

Normal saline 100mL(guess as 2㎍/mL):the infusion of 0.2㎍/kg/hr is started at 30 minutes before the procedure and the infusion dose is raised to 0.4㎍/kg/hr after completion of procedure

Sponsors

Severance Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* age ≥ 20, * ASA class I and II

Exclusion criteria

* bradycardia (\< 45 bpm) * heart block * liver failure * renal failure * uncontrolled hypertension * body mass index ≥ 30 kg/m2

Design outcomes

Primary

MeasureTime frame
Fentanyl consumption by patient-controlled analgesia24 hours

Secondary

MeasureTime frame
Side effects24 hours

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026