第四军医大学硕士学位论文
we designed this clinical trial, the purpose is to evaluate the efficacy and safety of two
kinds of UACE in the treatment of EP.
Objective:
To evaluate the efficacy and safety of two kinds of UACE in the treatment of EP.
Methods:
A single center, randomized, double-blind, controlled clinical trial was carried out. A
total of 50 cases of EP patients were randomly divided into the treatment group (perfusion
chemotherapy with MTX and 5-FU and embolization) or the control group(perfusion
chemotherapy with MTX and embolization) and were treated with two kinds uterine artery
perfusion chemotherapy and embolization. The primary efficacy endpoints were the serum
β-HCG value , the clinical healing time, the tubal patency rate after UACE. The adverse
events were recorded. Analysis of covariance, analysis of variance for repeated
measurement data, t test, and χ2 test were used for statistical analysis.
Results:
The differences between the two groups of serum β-HCG values on the main effect of
treatment method and time interaction were not statistically significant. The difference of
time effect of the two group was statistically significant.There was no significant
difference between control group (26.74±5.57 d) and treatment group (28.57±5.08 d) on
the clinical healing time. There was no significant difference between control group
(78.9%) and treatment group (76.2%) on the tubal patency rate. Two groups of
postoperative adverse events were mild,there was significant difference between control
group (26.1%) and treatment group (58.3%) on the incidence of adverse events.
Conclusion:
Two kinds of intervention methods have the same clinical curative effect, however,
the incidence of adverse events of control group is lower than treatment group. We
recommend using a signal MTX perfusion chemotherapy and embolization in the
treatment of ectopic pregnancy.
Key words:Ectopic pregnancy;Treatment;Uterine artery chemotherapy and embolization;
Methotrexate; 5-Fluorouracil
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