Actively Recruiting

Phase Not Applicable
Age: 20Years +
FEMALE
NCT04169451

IUI With Letrozole Versus in Natural Cycle

Led by Peking University Third Hospital · Updated on 2024-02-07

982

Participants Needed

1

Research Sites

191 weeks

Total Duration

On this page

Sponsors

P

Peking University Third Hospital

Lead Sponsor

T

The First Affiliated Hospital of Anhui Medical University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Rationale Intrauterine insemination (IUI) is the treatment of first choice for couples with unexplained and mild male factor infertility in many countries, but it is controversial whether ovarian stimulation improves fertility outcomes. In recent retrospectively collected data, we found that in couples with unexplained and mild male factor infertility undergoing IUI, ovarian stimulation with letrozole increased live birth rate as compared to natural cycle IUI without substantially increasing the multiple pregnancy rate. We therefore intend to perform a randomized clinical trial (RCT) on the subject in five reproductive medical centers in different cities in China. Objective To test the hypothesis that in couples with unexplained or mild male factor infertility scheduled for an IUI program ovarian stimulation with letrozole increases the live birth rate as compared to natural cycle treatment. Study design Multicenter randomized controlled trial. Study population Women diagnosed with unexplained or mild male factor infertility scheduled for treatment with IUI. Intervention Women will be randomized for ovarian stimulation with letrozole or to natural cycle IUI. In the group allocated to ovarian stimulation, women will receive oral tablets letrozole 5 mg daily from cycle day 3 for 5 days. We will treat the couples for 3 cycles, with a time horizon of 4 months. Main study parameters/endpoints Primary outcome is live birth resulting from conception within 4 months after randomization. Secondary endpoints are clinical pregnancy, multiple pregnancy, miscarriage rates, pregnancy complications, time to pregnancy leading to live birth. Nature and extent of the burden and risks associated with participation, benefit and group relatedness The strategies compared are already broadly applied in current practice. No additional risks are expected. There is no benefit for participants, but the results may benefit future infertile couples.

CONDITIONS

Official Title

IUI With Letrozole Versus in Natural Cycle

Who Can Participate

Age: 20Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with unexplained or mild male infertility
  • At least one fallopian tube open (tubal patency) confirmed by local protocol
  • Partner's semen quality normal or mildly impaired with total motile sperm count no less than 5 million based on recent analysis
Not Eligible

You will not qualify if you...

  • Woman has both fallopian tubes blocked
  • Women with irregular menstrual cycles, polycystic ovary syndrome (PCOS), or other endocrine disorders
  • Man with semen quality impaired: total motile sperm count less than 5 million

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Peking University Third Hospital

Beijing, Beijing Municipality, China, 100191

Actively Recruiting

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Research Team

S

Shuo Huang

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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