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Effect of intraarterial lidocaine on post uterine fibroma embolization pai

Phase 2
Recruiting
Conditions
Post-uterine artery embolization pain.
Registration Number
IRCT20220126053835N1
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
50
Inclusion Criteria

The patients with confirmed leiomyoma by ultrasonography
Being in the childbearing ages
Being the candidate of uterine artery embolization according to the opinion of obstetrician and gynecology specialist

Exclusion Criteria

The patients with medical history of hypersentivity to pethidine, morphine, lidocaine and contrast agents
The history of cardiac arrhythmia
The presence of active pelvic inflammatory disease

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Postoperative pain. Timepoint: 2, 4, 6 and 8 hours after the operation. Method of measurement: Visual Analogue Scale.;The applied pethidine dosage for pain controlling. Timepoint: 2, 4, 6 and 8 hours after the operaion. Method of measurement: According to the medical records (mg).
Secondary Outcome Measures
NameTimeMethod
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