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NCT Number: NCT02539290

Preovulatory Uterine Flushing With Saline as a Treatment for Unexplained Infertility

The purpose of this study is to determine whether preovulatory uterine flushing with physiological saline is effective in the treatment of unexplained infertility.

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This study is active but is not currently recruiting participants.

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Key information

Age range

18 year–37 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Centre Hospitalier Universitaire de Quebec

Québec, G1V 4G2, Canada

About this study

In vitro fertilisation is the only current reasonable treatment for unexplained infertility. Uterine flushing, associated with a five-fold increase in pregnancy when performed preovulatory, has been proposed as a new alternative. This treatment could flush out debris or alter inflammatory factors preventing fertilisation and implantation. The objective of this study is to assess the efficacy of pre-ovulatory uterine flushing with physiological saline for the treatment of unexplained infertility. This study is a randomised controlled trial based on consecutive women aged between 18 and 37 years consulting for unexplained infertility for at least one year. The day of their luteinizing hormone surge, 192 participants will be randomised in two equal groups to either receive 20 millilitres of physiological saline by an intra-uterine catheter or 10 millilitres of saline intravaginally. Investigators will assess relative risk of live birth (primary outcome), as well as pregnancy over one cycle of treatment. Side effects, complications, and acceptability of the intervention will be reported.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Primary or secondary infertility ≥12 months.
  • Diagnosis of unexplained infertility ≤24 months:
  • Anti-Mullerian hormone ≥0.4 ng/mL and/or follicle-stimulating hormone ≤13 IU/L in early follicular phase;
  • regular cycle of 21-35 days,
  • positive ovulation tests, and/or
  • luteal phase serum progesterone ≥25mmol/L in a natural cycle;
  • semen analysis with total motile sperm count ≥ 5 million;
  • normal uterine cavity;
  • patent tubes.
  • Negative genitourinary test for gonorrhoea and chlamydia ≤12 months.

Exclusion criteria

  • Body mass index ≥35 kg/m2.
  • Ongoing pregnancy.

Treatment and study plan

Detection of ovulation

Behavioral

Detecting the luteinizing hormone surge using test sticks in a urine sample

Uterine flushing

Procedure

Injection of 20 millilitres of physiological saline by an intra-uterine catheter the day of the luteinizing hormone surge

Other names: Tubal flushing

Vaginal flushing

Procedure

Injection of 10 millilitres of physiological saline intravaginally the day of the luteinizing hormone surge

Sexual intercourse

Behavioral

Sexual intercourse on the day of the intervention and the following day

Primary outcomes

  1. Proportion of participants with a live birth resulting from one cycle of treatment

    Time frame: 10 months after randomisation

    Proportion of participants with a live birth resulting from one cycle of treatment based on questionnaire and medical data.

Secondary outcomes

  1. Proportion of participants with a pregnancy resulting from one cycle of treatment

    Time frame: One month after randomisation

    Proportion of participants with a positive urinary or serum pregnancy test, gestational sac on ultrasound or histological evidence of trophoblastic tissue resulting from one cycle of treatment based on questionnaire and medical data.

  2. Adverse effects

    Time frame: One month after randomisation

    Number of participants with treatment-related pain, vagal symptoms, nausea, vomiting, temperature, pelvic infection

  3. Proportion of participants who find the intervention acceptable

    Time frame: One month after randomisation

    Proportion of participants that would be willing to receive the intervention for a second time and find the intervention acceptable.

Sponsors and collaborators

Lead sponsor

CHU de Quebec-Universite Laval

Other

Registry information

Official study title

Preovulatory Uterine Flushing With Saline as a Treatment for Unexplained Infertility: A Randomised Controlled Trial Protocol

Important dates

Study start
2015
Primary completion
2024
Study completion
2025
First posted
Sep 3, 2015
Registry last updated
Jan 13, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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