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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03862586
Other study ID # Royan-Genetics
Secondary ID
Status Completed
Phase Phase 3
First received
Last updated
Start date February 1, 2015
Est. completion date July 1, 2017

Study information

Verified date March 2019
Source Royan Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Comparison of the group treated with NAC-supplementation and placebo- administered groups showed elevations in HOXA cluster genes (all members) expression level in endometrium of women with RIF.


Description:

Despite significant developments in assistant reproductive technology (ART) that have overcome many underlying causes of infertility, pregnancy success rates remain relatively low, mainly due to implantation failure. Embryo quality and endometrial receptivity are two significant factors that believed to be the key points in implantation. Since recent studies that showed high expression of some HOXA genes affects on successful implantation rate, thus we examined the expression of HOXA genes in NAC supplementation during window of implantation (WOI) in women with (RIF). Also the effect of NAC on the improvement of implantation in RIF patients was investigated. Forty unfertile women with a diagnosis of RIF, referred to Royan Institute were included in the study. The study was of the type a single center, double blinded, placebo controlled, randomized trial. Expression of HOXA genes were assessed on the day of WOI (using Real Time PCR) biopsies from endometrium. Subjects randomly assigned to receive either NAC (A) or placebo (B) with both effervescent tablets having similar color, size and appearance. The patients were randomly categorized in two groups (A/B) to receive NAC 1200 mg/day or placebo, for at-least 6 weeks before starting ovarian stimulation. Pipelled-based biopsy from endometrium was done on specific day (19-21) of their cycle. Then patients were undergone ovarian stimulation (using NAC) ended to IVF treatment. RNA extraction and cDNA synthesis were performed from endometrium samples and then we evaluated expressions levels by Real-time PCR. Then we analyzed our data by independent Sample T-test and Mann-whitney U Test.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date July 1, 2017
Est. primary completion date May 1, 2017
Accepts healthy volunteers No
Gender Female
Age group 22 Years to 40 Years
Eligibility Inclusion Criteria:

1. Age between 20 and 40 years old

2. At least two IVF failure

3. BMI in the normal range

Exclusion Criteria:

1. Irregular menstrual cycle

2. Taking hormonal drugs except thyroid medication

3. Abnormal karyotype or chromosomal disorders

4. Coagulation problems.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
N-acetyl cysteine

Placebos


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Royan Institute

Outcome

Type Measure Description Time frame Safety issue
Primary Expression of HOXA in endometrium mRNA expression by quantitative PCR for homeo box A approximately 20 days after the first day of menstruation (each day is 28 days)
Secondary Positive pregnancy test Measurement of quantitative serum ß-hCG 16 days after embryo transfer
Secondary Endometrium thickness Endometrium thickness approximately 20 day after the first day of menstruation (each day is 28 days)
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