Uterine fibroid
Conditions
Interventions
Two groups:Vasopressin vs placebo, At the time of surgery only
Sponsors
North District Hospital, The Chinese University of Hong Kong
Eligibility
Sex/Gender
Male
Age
18 Years to 56 Years
Inclusion criteria
Inclusion criteria: Premenopausal women with symptomatic submucous fibroid will be recruited in the study. The diagnosis of submucous fibroid will be made by transvaginal ultrasound and diagnostic hysteroscopy. The size of the submucous fibroid will be measured by ultrasound. Hysteroscopic myomectomy will be performed for fibroids less than 5cm in size. The type of submucous fibroid will be determined by ultrasound and hysteroscopy using the Wamsteker classification(13).
Exclusion criteria
Exclusion criteria: Menopausal women, patients with endometrial premalignant or malignant pathologies, patients who require endometrial ablation, or on anticoagulant therapy, patients with cardiovascular diseases, migraine, asthma, heart failure, epilepsy and patients unwilling to participate will be excluded from the study. Women<18 years old will not be recruited.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Surgical time: cervical dilatation/myomectomy/poly;Fluid difference, intravasation of distending fluid; | — |
Secondary
| Measure | Time frame |
|---|---|
| Intraoperative blood loss;Drop in hemoglobin level;Complete excision;Intraoperative complication;Postoperative complication and Length of hospital stay; | — |
Countries
China
Contacts
Public ContactDr. Alyssa Sze Wai Wong
Outcome results
None listed