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You are here: Clinical Trials >
Information obtained from ClinicalTrials.gov on 2006-12-08 Link to the current ClinicalTrials.gov record. Condition(s) treated: Anovulation; Obesity Intervention: weight reduction minimal access surgery (Procedure) Enrollment status: Recruiting. Expecting to enroll 30 people. Sponsor: Sheffield Teaching Hospitals NHS Foundation Trust
Principal investigator(s) or official(s):
Overall contact:
This study will investigate the role of weight reduction surgery on the reproductive performance of obese women with ovulation problems. It is hypothesized that surgery offered when other methods of weight reduction have failed, may help restore ovulation.
Official title: The Effect of Weight Reduction Surgery on Ovarian Function in Obese Anovulatory Patients Study design: Observational, Natural History, Longitudinal, Defined Population, Prospective Study Detailed description: We aim to recruit 30 patients suffering from chronic anovulation, with a body mass index of 35 or more, who failed to achieve weight reduction with other methods such as orlistat, metformin, diet and exercise. Patients will be approached by one of the investigators in the infertility clinics and the assisted conception unit of the Royal Hallamshire hospital. Consent will be obtained by one of the designated investigators. The consent form has been designed in accordance with the guidelines of the central office for research and ethics committees (COREC). A patient information leaflet will be supplied and has been designed according to the COREC guidelines. Patients will have a baseline history, clinical examination, hormonal profile (FSH/LH, fasting Insulin/glucose ratio, androgen profile, day 21 serum progesterone, serum leptin and ghrelin levels) ultrasound examination (ovarian volume and antral follicle count), including Doppler blood flow study (ovarian stromal velocity). Patients will be offered laparoscopic gastric bypass surgery by Mr Roger Ackroyd, in line with the current recommendation for gastric surgery according to NICE guidelines i. e. patients with a BMI over 40 or a BMI over 35 with at least one co-morbidity. Patients will be reviewed monthly for six months. At each visit the following will be recorded: 1. Weight, menstrual diary. 2. Hormonal profile (FSH/LH, fasting Insulin/glucose ratio, androgen profile, day 21 serum progesterone, serum leptin and ghrelin levels). 3. Doppler of ovarian stroma (Pulsitility index, Peak velocity), ovarian volume and antral follicle count 4. Review of symptomatology especially androgenic symptoms. End point: Completion of six months follow up.
Minimum eligible age: 18 Years. Maximum eligible age: 45 Years. Eligible gender(s): Female. Criteria: Inclusion Criteria:
Dr Mostafa Metwally, MRCOG, Email: m.metwally@sheffield.ac.uk Jessop Wing, Royal Hallamshire Hospital, Sheffield S10 2SF, United Kingdom; Recruiting
Start date: February 2006
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