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Intrauterine Insemination With Letrozole Versus in Natural Cycle

Primary Purpose

Infertility, Intrauterine Insemination

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
letrozole
Sponsored by
Peking University Third Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infertility

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Being diagnosed with unexplained or mild male subfertility
  • At least one sided tubal patency, established according to local protocol
  • Normal or mild impairment of semen quality defined as a TMSC of 3 million or more based on at least one semen analysis

Exclusion Criteria:

  • Woman with double sided tubal pathology
  • Women with irregular cycles, PCOS or other endocrine disorders
  • Impaired semen quality: pre-wash TMSC <3 million.

Sites / Locations

  • Peking University third Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

letrozole group

natural cycle group

Arm Description

letrozole 5mg/day starting from day 3 of menstrual cycle for 5 days

Outcomes

Primary Outcome Measures

ongoing pregnancy
Primary outcome is ongoing pregnancy leading to live birth

Secondary Outcome Measures

Full Information

First Posted
February 25, 2018
Last Updated
February 5, 2021
Sponsor
Peking University Third Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03455426
Brief Title
Intrauterine Insemination With Letrozole Versus in Natural Cycle
Official Title
Intrauterine Insemination With Letrozole Versus Intrauterine Insemination in Natural Cycle. A Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Completed
Study Start Date
March 15, 2018 (Actual)
Primary Completion Date
June 30, 2019 (Actual)
Study Completion Date
December 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Peking University Third Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
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, investigators 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. Investigators therefore perform a randomized clinical trial (RCT) on the subject in the Centre of Reproductive Medicine, Peking University Third Hospital, Beijing, 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 Randomized clinical 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 3-5 for 5 days. Investigators will treat the couples for 3 cycles, with a time horizon of 4 months. Main study parameters/endpoints Primary outcome is ongoing pregnancy leading to live birth. Secondary endpoints are clinical pregnancy, multiple pregnancy, miscarriage rates, pregnancy complications and patients' costs. 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 subfertile couples.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility, Intrauterine Insemination

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
letrozole group
Arm Type
Experimental
Arm Description
letrozole 5mg/day starting from day 3 of menstrual cycle for 5 days
Arm Title
natural cycle group
Arm Type
No Intervention
Intervention Type
Drug
Intervention Name(s)
letrozole
Intervention Description
Women will be randomizedfor ovarian stimulation with letrozole or to natural cycle IUI.
Primary Outcome Measure Information:
Title
ongoing pregnancy
Description
Primary outcome is ongoing pregnancy leading to live birth
Time Frame
3 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Being diagnosed with unexplained or mild male subfertility At least one sided tubal patency, established according to local protocol Normal or mild impairment of semen quality defined as a TMSC of 3 million or more based on at least one semen analysis Exclusion Criteria: Woman with double sided tubal pathology Women with irregular cycles, PCOS or other endocrine disorders Impaired semen quality: pre-wash TMSC <3 million.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shuo Huang, PhD
Organizational Affiliation
Peking University Third Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Peking University third Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100191
Country
China

12. IPD Sharing Statement

Citations:
PubMed Identifier
36165742
Citation
Franik S, Le QK, Kremer JA, Kiesel L, Farquhar C. Aromatase inhibitors (letrozole) for ovulation induction in infertile women with polycystic ovary syndrome. Cochrane Database Syst Rev. 2022 Sep 27;9(9):CD010287. doi: 10.1002/14651858.CD010287.pub4.
Results Reference
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Intrauterine Insemination With Letrozole Versus in Natural Cycle

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