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The Impact of Having a Tattoo on Fertility Treatment Outcome

The Impact of Having a Tattoo on Fertility Treatment Outcome: A Prospective Randomized Controlled Trial

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07405879
Enrollment
328
Registered
2026-02-12
Start date
2026-02-10
Completion date
2031-01-28
Last updated
2026-02-12

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

Conditions

Assisted Reproductive Technology Outcomes, Infertility

Keywords

In vitro fertilization, Embryo transfer, Live birth, pregnancy, Assisted reproductive technology, Tattoos, Chronic inflammation

Brief summary

Tattoos are increasingly common among women of reproductive age, yet their potential systemic inflammatory effects and impact on fertility treatment outcomes are unknown. This prospective observational cohort study aims to evaluate whether the presence, size, duration, and ink characteristics of tattoos are associated with pregnancy outcomes following embryo transfer in women undergoing in vitro fertilization (IVF).

Detailed description

This is a single-center, prospective observational cohort study conducted at the McGill University Health Centre Reproductive Centre. Women undergoing IVF with planned fresh or frozen blastocyst embryo transfer will be enrolled and categorized based on tattoo presence and characteristics. Tattoo information will be collected using a standardized questionnaire and direct measurement. Participants will be followed for pregnancy and obstetric outcomes through medical chart review. The primary outcome is ongoing pregnancy rate following embryo transfer. Secondary outcomes include clinical pregnancy, biochemical pregnancy, miscarriage, ectopic pregnancy, and live birth.

Interventions

None listed

Sponsors

McGill University Health Centre/Research Institute of the McGill University Health Centre
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
21 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

Women aged 21-40 years Undergoing IVF with planned fresh or frozen blastocyst embryo transfer Availability of good-quality blastocyst embryos Willingness to provide informed consent

Exclusion criteria

Significant untreated uterine abnormalities ≥3 prior failed embryo transfers Hydrosalpinx in situ BMI \>40 kg/m² Age \>41 years at embryo creation Submucosal fibroids in situ Use of medications affecting implantation (e.g., chronic steroids, metformin)

Design outcomes

Primary

MeasureTime frameDescription
Ongoing Pregnancy Rate12 weeks gestationPresence of fetal heartbeat on ultrasound at ≥12 weeks

Secondary

MeasureTime frameDescription
Clinical pregnancy rate6-8 weeks of gestationpresence of a gestational sac
Biochemical pregnancy4-5 weeks of gestationpositive BHCG test
Miscarriage ratebefore the 20th week of pregnancyThe spontaneous loss of a fetus
Ectopic pregnancy rateupto 10 weeks of gestationthe frequency at which a fertilized egg implants outside the uterine cavity
Live birth rateover 23 weeks of gestationthe frequency of successful deliveries resulting in at least one live-born infant

Countries

Canada

Contacts

CONTACTmichael haim dahan, MD
thedoctormichaeldahan@gmail.com+14389907707
CONTACTmaya shavit, MD
maya.genel@gmail.com+14385963979
PRINCIPAL_INVESTIGATORmichael haim dahan, MD

McGill University Health Centre/Research Institute of the McGill University Health Centre

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026