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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03748238
Other study ID # 201871
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 1, 2018
Est. completion date January 2019

Study information

Verified date January 2019
Source Gurgan Clinic
Contact Timur Gurgan, MD,Professor
Phone 0905322317706
Email tgurgan@gurganclinic.com.tr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to investigate that the efficacy of the endometrial injury before IVF in recurrent implantation failure patients.


Description:

This is a prospective and randomized controlled trial investigating the effect of hysteroscopic endometrial injury for treatment of recurrent implantation failure. Approximately 230 patients who had failed to achieve a clinical pregnancy after the transfer of at least four good-quality embryos in a minimum of three fresh or frozen cycles to a woman under the age of 40 years will be randomized into two groups. Injury group will receive endometrial injury during their hysteroscopic procedure, whereas the control group (n=115) did not. This study will investigate that, whether the endometrial injury is beneficial in recurrent implantation failure patients to increase the odds of clinical pregnancy rates, live birth rates, and implantation rates.


Recruitment information / eligibility

Status Recruiting
Enrollment 230
Est. completion date January 2019
Est. primary completion date January 2019
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Women under the age of 40 who met the RIF definition

- Patients whose follicle-stimulating hormone (FSH) levels were = 15 IU/mL

Exclusion Criteria:

- Patients with congenital uterine anomalies

- Patients with Asherman's syndrome

- Patients with uterine cavity distorted by myoma or endometrial polyps

- Patients with confirmed endometriosis or endometrioma

- Patients with BMI of <18.5 and >29.9

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Endometrial Injury with Hysteroscopy
All office hysteroscopy procedures will be done transvaginally under sedation with a 5 mm 30 degree lens supplied with a 5 F working channel continuous flow office hysteroscope (Bettocchi office hysteroscope, Karl Storz, Tuttlingen, Germany) without speculum or tenaculum. Briefly, following cervical passage and initial endometrial cavity investigation endometrial injury will be performed without energy modality (i.e. with scissors). Endometrial injury will perform first on the fundus by cutting into the endometrium (without injuring the myometrium) transversally. Later, vertical incisions will perform 0,5 cm apart each other, on the anterior and posterior walls of the uterus, 1-1.5 cm away from the fundus and one cut for each lateral wall

Locations

Country Name City State
Turkey Gurgan Clinic IVF and Women Health Center Ankara Cankaya

Sponsors (1)

Lead Sponsor Collaborator
Gurgan Clinic

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Positive Pregnancy Blood concentration of beta-hcg 1month
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