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evaluation of hysteroscopic effect on endometrial receptivity of the patients in the IVF cycle

Randomised clinical trial of comparison between with and without atraumatic hysteroscopy on the emprovement of endometrial receptivity on the shariati hospitals patient in 1394

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016011022795N2
Enrollment
250
Registered
2016-03-04
Start date
2015-04-21
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infertility. Female infertility associated with anovulation,Female infertility of tubal origin,Female infertility of other origin,Female infertility, unspecified,

Interventions

Intervention 1: Performing hysteroscopy in the 5-7 days of the IVF cycle treatment and uterine irrigation with normal saline in the patients in intervention group . For patients in the control group d
Treatment - Other
Treatment - Drugs
Performing hysteroscopy in the 5-7 days of the IVF cycle treatment and uterine irrigation with normal saline in the patients in intervention group . For patients in the control group did not add any i
In the control group the traditional IVF cycle will be done without any additional intervention

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:regular mense;age less than 40;BMI=19-30;without any prior hysteroscopy examination or previous IVF or ICSI; with a normal Transvaginal sonography (TVS) (in the day 2-3 same cycle);normal hystrosalpingo graphy (HSG) (between 6to24 mounths) . Exclusion criteria : recurrent miscamiage (3 or more miscarriage); inter menstrual bleeding; any doubt about uterine cavity abnormality; server male factor request to PESA or TESE; patients with poly cystic ovary syndrome or endometriosis ;hydrosalpinx ;ovarian cyst ; cancellation of the same cycle for any reason

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Clinical pregnancy rate in two groups. Timepoint: 4 weeks after embryo transfer transvaginal sonography will be done and gestatinal sac will be evaluated. Method of measurement: Find gestational sac on transvaginal sonography.

Secondary

MeasureTime frame
Chemical pregnancy rate in two group ,abortion , implantation rate in two groups. Timepoint: two weeks after transfer for biochemical pregnancy,4weeks for clinical pregnancy,12 weeks after transfer for abortion,two weeks after transfer for implantation rate. Method of measurement: BHCG for biochemical ,trans vaginal sonography for clinical,physical examination and trans vaginal sonography for abortion ,trans vaginal sonography for implantation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarzieh Ghasemi

Tehran University of Medical Sciences,infertility ward

drghasemim@yahoo.com ghasemi-ma@razi.tums.ac.irghasemim841@yahoo.com+98 21 84901

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 13, 2026