No Condition Clinical Trial
Official title:
Comparison of Clinical Outcomes Between in Vitro Maturation and Minimal Stimulation in Vitro Fertilization in Patients With Polycystic Ovarian Syndrome; Prospective, Randomized Controlled, Parallel, Open-label, Clinical Trial
NCT number | NCT03134482 |
Other study ID # | Chau |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | May 1, 2017 |
Est. completion date | December 31, 2023 |
Polycystic ovarian syndrome (PCOS) is most common endocrinologic disease in women of
reproductive age with incidence of 6.6 ~ 8%. About fifty percent of the patients with PCOS
manifest subfertility and significant proportion of these woman need assisted reproductive
technology (ART). These patients are very sensitive to gonadotropins during conventional in
vitro fertilization (IVF) and the risk of ovarian hyperstimulation syndrome (OHSS) is high.
In vitro maturation (IVM) is an emerging alternative option to conventional IVF for
minimizing the risk of OHSS in patients with PCOS. Until now, several studies has been
reported the favorable outcomes of oocyte maturation rate, fertilization rate, clinical
pregnancy rate, and live birth rate during IVM procedure. However, these results were from
retrospective or observational study and there was no suitable randomized controlled trial
(RCT).
Therefore, this prospective RCT is aimed to compare and analyze the clinical outcomes between
IVM and minimal stimulation IVF in women with PCOS, assessing if IVM is recommendable
clinical practice or not.
Status | Recruiting |
Enrollment | 240 |
Est. completion date | December 31, 2023 |
Est. primary completion date | December 31, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 20 Years to 39 Years |
Eligibility |
Inclusion Criteria: - Women diagnosed with PCOS under age of 40 years (PCOS diagnosis is based on Revised 2003 Rotterdam criteria of PCOS) Exclusion Criteria: - severe male factor subfertility requiring testicular sperm extraction (TESE) or oligoasthenoteratozoospermia - couples requiring preimplantation genetic screening or diagnosis - women had undergone ovarian stimulation 30 days before assisted reproductive technology (ART) - women with severe endometriosis or dysfunctional uterine bleeding - women with severe uterine factor subfertility (ex. submucosal myoma, intramural myoma protruding endometrium, severe intrauterine adhesion, etc) - women with ovarian malignancy - women with severe tubal factor subfertility (ex. persistent hydrosalpinx even after surgery) - women had undergone treatment of malignancy 5 years before screening of this trial - women with history of thromboembolism - women with age of 40 years or more - women with stimulation dose over 150 IU of exogenous FSH |
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | CHA Fertility Center, Seoul station | Seoul | |
Korea, Republic of | CHA Gangnam medical center | Seoul |
Lead Sponsor | Collaborator |
---|---|
CHA University |
Korea, Republic of,
Aboulghar MA, Mansour RT. Ovarian hyperstimulation syndrome: classifications and critical analysis of preventive measures. Hum Reprod Update. 2003 May-Jun;9(3):275-89. Review. — View Citation
Cha KY, Chung HM, Lee DR, Kwon H, Chung MK, Park LS, Choi DH, Yoon TK. Obstetric outcome of patients with polycystic ovary syndrome treated by in vitro maturation and in vitro fertilization-embryo transfer. Fertil Steril. 2005 May;83(5):1461-5. — View Citation
Chian RC, Buckett WM, Tulandi T, Tan SL. Prospective randomized study of human chorionic gonadotrophin priming before immature oocyte retrieval from unstimulated women with polycystic ovarian syndrome. Hum Reprod. 2000 Jan;15(1):165-70. — View Citation
Child TJ, Phillips SJ, Abdul-Jalil AK, Gulekli B, Tan SL. A comparison of in vitro maturation and in vitro fertilization for women with polycystic ovaries. Obstet Gynecol. 2002 Oct;100(4):665-70. — View Citation
Choi MH, Lee SH, Kim HO, Cha SH, Kim JY, Yang KM, Song IO, Koong MK, Kang IS, Park CW. Comparison of assisted reproductive technology outcomes in infertile women with polycystic ovary syndrome: In vitro maturation, GnRH agonist, and GnRH antagonist cycles. Clin Exp Reprod Med. 2012 Dec;39(4):166-71. doi: 10.5653/cerm.2012.39.4.166. Epub 2012 Dec 31. — View Citation
Reavey J, Vincent K, Child T, Granne IE. Human chorionic gonadotrophin priming for fertility treatment with in vitro maturation. Cochrane Database Syst Rev. 2016 Nov 16;11:CD008720. Review. — View Citation
Siristatidis CS, Vrachnis N, Creatsa M, Maheshwari A, Bhattacharya S. In vitro maturation in subfertile women with polycystic ovarian syndrome undergoing assisted reproduction. Cochrane Database Syst Rev. 2013 Oct 8;(10):CD006606. doi: 10.1002/14651858.CD006606.pub3. Review. Update in: Cochrane Database Syst Rev. 2018 Nov 15;11:CD006606. — View Citation
Söderström-Anttila V, Mäkinen S, Tuuri T, Suikkari AM. Favourable pregnancy results with insemination of in vitro matured oocytes from unstimulated patients. Hum Reprod. 2005 Jun;20(6):1534-40. Epub 2005 Feb 3. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Clinical pregnancy rate | Clinical pregnancy was determined by observation of a gestational sac with fetal heart beat by transvaginal ultrasound scan. | At 6 weeks of pregnancy | |
Secondary | Incidence rate of Ovarian hyperstimulation syndrome (OHSS) | OHSS rate in each arm. Patients' symptoms (abdominal distension, bloating and pain, nausea, vomiting, palpitation) and ultrasonographic findings (fluid collection in pelvic and abdominal cavity, enlarged ovarian size) are investigated for OHSS detection. | Until three weeks later after hCG injection |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02265224 -
Bioequivalence Study of Two Different Formulations of N-acetyl-cysteine (NAC)
|
Phase 1 | |
Completed |
NCT00379210 -
Neural Effects of Mindfulness Training on Attention
|
N/A | |
Completed |
NCT05901220 -
Joint School-Health Project of the Neapolitan Child
|
N/A | |
Active, not recruiting |
NCT04455295 -
Testing the Noradrenergic Hypothesis of Transcutaneous Vagus Nerve Stimulation
|
N/A | |
Not yet recruiting |
NCT03225638 -
Performance Evaluation by Magnetic Resonance Imaging (MRI) of Intramuscular Thigh Injections With 3 Configurations of Needle-free Injector (ZENEO®)
|
N/A | |
Completed |
NCT04854642 -
A Single Dose Study About the Influence of Food on the Oral Bioavailability of Ladarixin Capsule in Healthy Volunteers
|
Phase 1 | |
Terminated |
NCT04803396 -
Ascending Dose Tolerability Trial and PK Assessment in Healthy Volunteers After Single & Multiple Oral Intake of DF2755A
|
Phase 1 | |
Completed |
NCT05882942 -
Matcha Green Tea Effects at Rest and During Moderate-intensity Exercise in Females
|
N/A | |
Completed |
NCT03044301 -
Performance Thresholds Evaluation by Wet Injection Quantification and Magnetic Resonance Imaging (MRI) of Subcutaneous and Intramuscular Injections (0,65ml) of Several Configurations of Needle-free Devices (ZENEO®)
|
N/A | |
Completed |
NCT01563224 -
GABA-B Receptor Function in Healthy Volunteers
|
N/A | |
Terminated |
NCT04227405 -
TOGETHER: A Couple's Model to Enhance Relationships and Economic Stability
|
N/A | |
Completed |
NCT04802967 -
A Study on Ketoprofen Lysine Salt (KLS) + Gabapentin (GABA) vs KLS to Investigate Their Pharmacodynamic in Healthy Males
|
Phase 1 |