The Effect of Growth Hormone in Assisted Reproductive Technology Clinical Outcome of Poor Responder

Low Ovarian Reserve Clinical Trial

Official title:

A Pilot Study of the Effect of Growth Hormone in Assisted Reproductive Technology Clinical Outcome of Poor Responder

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03027843
• Other study ID #: newivf20170110
• Status: Not yet recruiting
• Phase: Phase 4
• First received: January 13, 2017
• Last updated: January 19, 2017
• Start date: March 2017
• Est. completion date: April 2020

Study information

• Verified date: January 2017
• Source: Sun Yat-sen University
• Contact: Xing Yang, M.D. & Ph.D.
• Phone: 020-38048013
• Email: yxing_8358[@]126.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Assisted reproduction treatment in patients with low ovarian reserve is a big difficult clinical problem. Growth hormone (GH) is crucial in the development of follicles since preantral follicle to ovulation and can promote steroid hormones and gamete formation, increase the granular cell sensitivity,and inhibition of follicular atresia. Latest research shows that GH can improve egg quality through regulating mitochondrial function of the oocytes and increase the rate of embryo euploid. It becomes a new argument in that promotion of clinical pregnancy rate in assisted reproduction treatment. GH applied in the field of assisted reproduction 30 years experience of applicable people, but drug dosage, drug intervention time continue to explore. 2015 China assisted reproductive stimulate ovulation medicine expert consensus recommend joint GH for poor ovarian response, repeated implantation failure patients and older patients assisted fertility treatment, but not on the specific use time limit, the daily dose of drugs and curative effect. How to maximize growth hormone potential advantage in improving the egg quality bothers the clinical doctors. We had a self-controlled retrospective analyses in growth hormone application and found that the average daily injections of GH dose 2 iu for 45 days can significantly improve the embryo quality in patients with low ovarian reaction. And now long-acting recombinant human growth hormone is available, which make it convenient for patients. A forward-looking experimental is expected to answer clinical practical problems and provide proper GH regimen for low ovarian responder.

Description:

This study is a pilot study to investigate the effect of growth hormone in assisted reproductive technology clinical outcome of poor responder.

Design: randomized controlled trial. Setting: Assisted reproductive technologies unit. Patients: patients diagnosed poor ovarian responder who is in accordance with the inclusion criteria, and not meet the exclusion criteria, who had repeated IVF treatment from Mar 2017 to Aug 2019.

Intervention: The comparison was made between GH group and the control group, both groups are conducted with the mini-dose GnRH-a long protocol for IVF treatment. GH group use Long-acting recombinant human growth hormone 14IU qw, until the day of hCG.

Main outcome measures: The primary outcome of the study is live birth rate. The secondary outcomes were clinical pregnancy rate, number of oocytes retrieved, fertility rate, normal fertilization rate, rate of transferable embryo and good quality embryo rate.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 80
• Est. completion date: April 2020
• Est. primary completion date: August 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 30 Years to 40 Years

Eligibility

Inclusion Criteria:

1. Women age =35 years and =40 years.

2. 2= AFC=6, and AMH level =0.5 and= 1.1 ng/ml.

3. Previous failed transfer cycle =2

4. Didn't participate in other clinical subjects in three months.

5. Written informed consent.

Exclusion Criteria:

1. Body mass index (BMI) =25 kg/m2.

2. Endocrine metabolic disease, such as diabetes, insulin resistance, hyperthyroidism, Cushing's syndrome, hyperprolactinemia.

3. Hypertension (systolic blood pressure =140mmHg and diastolic blood pressure=90mmHg.

4. Autoimmune diseases was definitively diagnosed, such as systemic lupus erythematosus, Sjogren's syndrome, Hashimoto's Thyroiditis, multiple sclerosis, rheumatoid arthritis, autoimmune hemolytic anemia, recurrent miscarriage.

5. Ovarian neoplasm that =4 cm in diameter and has no clear pathological diagnosis by surgery.

6. Complicated with adenomyosis, endometriosis confirmed by surgery, ovarian endometriosis cyst =2 cm by ultrasound, all kind of malignant tumors or precancerous disease.

7. Untreated hydrosalpinx.

Eliminate or falls off Criteria:

1. Withdraw drug and take appropriate treatment measures if serious adverse events happen during the trial, and subjects will be off.

2. Patients that have bad compliance.

3. Subjects are found breach the inclusion criteria, or in accordance with exclusion criteria during the test, excluded.

4. Patients request withdrawal and exit the trial because adverse events occur during the trial.

5. No record about treatment.

Related Conditions & MeSH terms

• Low Ovarian Reserve

Intervention

Drug:
• Growth Hormone
in GH group, patients have weekly injections of GH dose 14 iu, until the day of hCG.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Sun Yat-sen University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	live birth rate	Live birth rate(%): number of live birth/ transferred cycle.Compare the live birth rate between the two group with SPSS 20.0.	1-2year
Secondary	clinical pregnancy rate	Clinical pregnancy means pregnancy sac is seen intrauterine under ultrasound 7 weeks after embryo transferred. Clinical pregnancy rate(%): number of clinical pregnancy/transferred cycle.Compare the clinical pregnancy rate between the two group with SPSS 20.0.	1-2 year
Secondary	number of oocytes retrieved	Compare the number of oocytes retrieved between the two group with SPSS 20.0.	1-2 year
Secondary	fertility rate	Fertility rate(%): number of occyte fertilized/ number of oocytes retrieved. Compare the fertility rate between the two group with SPSS 20.0.	1-2 year
Secondary	normal fertility rate	Normal fertility rate(%): number of occyte normally fertilized/ number of oocytes retrieved. Compare the normal fertility rate between the two group with SPSS 20.0.	1-2 year
Secondary	transferable embryo rate	Cleavage embryo grades 1 or 2 with at least 5 blastomeres are considered as transferrable embryo.Transferable embryo rate(%): number of transferable embryo/number of feritilized oocytes. Compare the transferable embryo rate between the two group with SPSS 20.0.	1-2 year
Secondary	good quality embryo rate	Cleavage embryo grades 1 or 2 with 6-10 blastomeres were considered good quality embryos. Good quality embryo rate(%): number of good quality embryo/number of feritilized oocytes.Compare the good quality embryo rate between the two group with SPSS 20.0.	1-2 year