Fibroid
Conditions
Keywords
Fibroid, Ulipristal, Selective progesterone receptor modulator, Chinese
Brief summary
Uterine leiomyomas is the commonest benign tumour of the female genital tract. It lead to menorrhagia, anaemia, pain and pressure symptoms. Due to the enlarged uterus, the use of minimal invasive surgery is limited. There is also increase risk of intraoperative blood transfusion. Ulipristal acetate (UPA) is a selective progesterone-receptor modulator (SPRM). Preoperative use of Ulipristal for 12 weeks has been shown to decrease uterine bleeding, fibroid volume, pre-operative anaemia and symptoms severity. However there is still lacking evidence in terms of long term safety and efficacy, especially in Chinese population. The aim of the present study is to evaluate the effect and safety on preoperative use of Ulipristal on fibroid.
Detailed description
Uterine leiomyomas is the commonest benign tumour of the female genital tract. It is often asymptomatic, but can also lead to anaemia, pain and pressure symptoms. It is the commonest indication for hysterectomy, especially abdominal hysterectomy. Currently, the use of hormonal treatment is associated with side effects including gastrointestinal upset, bloating, weight gain and thromboembolic risks. The main stay for treatment relies on surgery. Furthermore, the use of minimal invasive surgeries is limited by the size of the fibroids. Preoperative use of Gonadotrophic Releasing Hormone analogues (GnRHa) is effective in shrinkage of the uterine leiomyomas and reduction of uterine bleeding. However, postmenopausal symptoms including hot flushes, vaginal dryness are profound. Ulipristal acetate (UPA), previously named CDB-2914, is a selective progesterone-receptor modulator (SPRM). It binds to the progesterone receptors with high affinity. It inhibits follicular development and ovulation, while it has no significant effects on estradiol levels and antiglucocorticoid activity. Preoperative use of Ulipristal for symptomatic uterine fibroids has been investigated in randomized controlled study with improvement in terms of uterine bleeding, fibroids volume, pre-operative anaemia and symptoms severity. However there is still lacking evidence in terms of long term safety and efficacy. Also there is lack of evidence in Chinese population. The aim of the present study is to evaluate the effect and safety on preoperative use of Ulipristal on fibroid.
Interventions
DRUGUlipristal acetate
Ulipristal acetate 5mg daily will be prescribed
OTHERPlacebo pills
Placebo pills will be prescribed
DRUGFerrous sulphate
Ferrous sulphate 300mg three times a day will be prescribed if haemoglobin level is less than 10g/dL.
DRUGTranexamic Acid
Tranexamic Acid 500mg four times a day on request basis will be prescribed if patient complained of menorrhagia.
Sponsors
Queen Mary Hospital, Hong Kong
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Scheduled for hysterectomy for symptomatic fibroid * Be a Chinese * Pre-menopausal * With a Pictorial bleeding assessment chart score \> 100 during menstruation at the preceding month * Non-pregnant * With a body-mass index between 18 to 30.
Exclusion criteria
* History of uterine surgery (apart from Caesarean section or cervical conization), endometrial ablation or uterine artery embolization * History of gynaecological malignancies * History of endometrial hyperplasia * Known haemoglobinopathy (e.g. thalassaemia) * Known severe coagulation disorder * Has one or more ovarian cysts \>= 4 cm in diameter diagnosed by ultrasound * History of use of Selective Progesterone Receptor Modulator (SPRM) * Current (within 12 months) problem with alcohol or drug abuse. * Known allergy to SPRM or ferrous sulphate
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change of uterine bleeding | Through study completion, an average of 14weeks | Pictorial bleeding assessment chart will be used for assessment of uterine bleeding. Patients will be assessed before the start of treatment, after completion of 6 weeks course and after completion of 12 weeks course. The change of uterine bleeding after completion of 12 weeks course of treatment will be recorded. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change of fibroid volume | Through study completion, an average of 14weeks | The fibroid volume will be measured using ultrasonography before start of treatment, after 6 weeks course of treatment and after completion of 12 weeks course of treatment. |
| Intraoperative blood loss | After completion of 12 weeks course, the intraoperative blood loss at the time of performance of hysterectomy will be assessed. | The amount of blood loss at hysterectomy will be recorded. |
| Side effects | Through study completion, an average of 14weeks | The side effects including nausea, vomiting, headache, dyspepsia will be recorded. |
| Change of haemoglobin level | Through study completion, an average of 14weeks | The change of haemoglobin level after completion of 12 weeks course will be recorded. |
| Histology of the operative specimen | After completion of 12 weeks course of treatment | Presence of malignancy or hyperplasia in the operative specimen will be recorded. |
| Conversion to less invasive intervention options | After completion of 12 weeks course of treatment and before the scheduled operation | 2 weeks before scheduled operation, patients will be assessed by the operation team and the most suitable route of hysterectomy will be discussed again. The possibility of conversion to less invasive intervention options including from laparotomy to laparoscopy will be recorded. |
Countries
Hong Kong
Outcome results
None listed