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Completed

NCT Number: NCT06178523

Cost-effective Treatment of Unexplained Infertility

The issue of unexplained infertility that Southam brought up in 1960 is still a problem today. Despite improvements in infertility assessment, many couples still don't know why they are infertile. Even with the use of the most advanced ovulation detectors, fallopian tube patency tests, and semen evaluations, competency cannot identify every potential flaw in the intricate processes leading to conception. Unexplained infertility will be a challenge for both biological and clinical researchers since it results from these gaps in our understanding of fertilization and from our incapacity to use all of the current evidence-based information.

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Key information

Age range

18 year–35 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 4

Primary location

Batterjee Medical College

Jeddah, Mecca Region, 21442, Saudi Arabia

About this study

For the treatment of unexplained infertility, Clomiphene Citrate (CC) is frequently used either alone or in conjunction with intrauterine insemination (IUI). Its combined oestrogenic and anti-oestrogenic characteristics serve as the basis for the mechanism of action. When clomiphene citrate is used, the uterine blood flow is reduced during the peri-implantation stage of early luteal phase. About 80% of women experience ovulation, which has a cumulative effect over 6 to 8 months, yet the pregnancy rate in these women can still be relatively low. The endometrial and cervical mucus-level anti-oestrogenic actions of CC are the potential culprits. Without a doubt, one of the biggest obstacles in treating infertility is the endometrial impact. If the endometrial thickness (ET) is less than 6 mm, the pregnancy rate may be extremely low.

Sildenafil citrate promotes endometrial thickness and uterine blood flow. The capacity of the blastocyst to penetrate the endometrium and establish a lasting blood supply is crucial for successful implantation. To do this, the blastocyst needs genes in order to create the required proteins for breaking down the endometrial cellular matrix, control cell development, and trigger angiogenesis.

It can be difficult to understand the evidence on the efficacy and security of therapy for unexplained infertility. Given the substantial proportion of unaided pregnancies with expectant management, it is problematic that most studies do not include a placebo or untreated control group.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Saudi women.
  • Married women in a stable, continuous, unprotected heterosexual relationship (cohabitating with their husbands).
  • Aged between 18 to 35 years old.
  • Non-smoking.
  • Non-alcohol drinking.
  • With a body mass index < 30 Kg/M2,
  • Who are looking healthy (all their infertility-workup investigations including male partners' seminal analysis were within normal range)
  • Failed to conceive spontaneously within 2 years of marriage without evident cause (cases with primary infertility).

Exclusion criteria

  • All non-Saudi women,
  • Saudi unmarried women (not yet engaged in sexual activity),
  • Married women with age less than 18 or more than 35 years old,
  • Patients with secondary infertility,
  • Cigarette smokers.
  • Alcohol drinking.
  • BMI > 30 Kg/M2,
  • Pregnant women.
  • Breastfeeding women.
  • With known pathological cause (either male or female factor),
  • With hypersensitivity to any of medication planned to be used in the study.

Treatment and study plan

Clomiphene Citrate.

Drug

Clomiphene Citrate (Clomid®) 100 mg for 5 days starting from the second day of the menstrual cycle (Groups A, B, and C).

Other names: Clomid®

sildenafil citrate

Drug

Sildenafil Acetate (Viagra®) 25 mg as a vaginal tablet 6 hourly for 10 days starting from the fifth day of the menstrual cycle (Group-A).

Other names: Viagra®

Intrauterine Insemination

Procedure

IUI (Group-B).

Other names: IUI

Primary outcomes

  1. Pregnancy outcome

    Time frame: 7 weeks after positive pregnancy test.

    Ultrasound confirmation of intrauterine fetal heartbeat.

Sponsors and collaborators

Lead sponsor

Batterjee Medical College

Other

Registry information

Official study title

Cost-effective Treatment of Unexplained Infertility: A Prospective Multicenter, Double-blinded, Randomised Controlled Study

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Dec 21, 2023
Registry last updated
Feb 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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