Overview
L-carnitine and COH in PCOS Women Undergoing IVF/ICSI Cycles
Status:
Recruiting
Recruiting
Trial end date:
2022-10-01
2022-10-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
The aim of this study was to evaluate the effect of oral L-carnitine supplementation during controlled ovarian stimulation (COS) in patients with polycystic ovary syndrome (PCOS) in a double-blind randomized clinical trial. The eligible patients with PCOS diagnosis (on the basis of Rotterdam criteria) who referred to Royan Research Institute for IVF / ICSI treatment cycles will be evaluated.Phase:
N/AAccepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Royan Institute
Criteria
Inclusion Criteria:• Patients between 20 to 37 years old, presenting with primary or secondary infertility
following regular intercourse for at least 1 year and diagnosed with polycystic ovary
syndrome (PCOS) according to Rotterdam's criteria who had received two to three failures of
IUI cycle therapy were included. The diagnosis was based on a complete history taking,
physical examination and a paper documented complete infertility work-up within the
previous 6 months
Exclusion Criteria:
1. Patients diagnosed with hyperprolactinemia, diabetes mellitus, epilepsy
2. Patients treated with special diet, medication supplement (ovuboost), metformin before
or during ovarian stimulation
3. History of pelvic surgery on ovaries and uterus.
4. Presence of submucosal and intramural fibroids larger than 5 cm or the presence of
uterine polyps and congenital uterine malformations.
5. The cause of severe male infertility (TESE, PESA).