Actively Recruiting

Phase 4
Age: 18Years - 37Years
FEMALE
ID07185724

Balancing Comfort and Success: Post-retrieval Ketorolac in Fresh Embryo Transfers

Led by Jessica D. Kresowik · Updated on 2025-12-15

200

Participants Needed

1

Research Sites

48 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the use of ketorolac, a medication often used for pain relief after surgery, in patients undergoing in vitro fertilization (IVF) who plan to have a fresh embryo transfer five days after egg retrieval. The study aims to determine if giving ketorolac intravenously after egg retrieval affects important IVF outcomes such as implantation and live birth rates. This is a double-blind randomized controlled trial addressing concerns about ketorolac's effects on bleeding and embryo implantation. Participants will be randomly assigned to receive either 30 mg of ketorolac through an IV immediately after egg retrieval while still under sedation or no ketorolac at all, with all other IVF care remaining the same. The embryo transfer will occur on day five post-retrieval as planned. The trial uses a 1:1 randomization method and includes patients undergoing standard ovarian stimulation protocols. During the study, researchers will collect extensive medical and reproductive history as well as treatment details from medical records for up to 45 weeks. They will monitor pain levels, narcotic use, time to discharge, need for additional evaluations for pain or bleeding, and IVF outcomes including implantation, clinical pregnancy, miscarriage, and live birth rates. The primary outcome is the implantation rate confirmed by ultrasound about six weeks after egg retrieval.

CONDITIONS

Brief Title

Ketorolac Use and Fresh Embryo Transfer Outcomes

Who Can Participate

Age: 18Years - 37Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • IVF using own eggs (autologous oocytes) and all sperm sources
  • IVF cycles using ICSI or standard insemination
  • Plan to transfer embryo on day 5 after retrieval
  • Body mass index (BMI) below 50
Not Eligible

You will not qualify if you...

  • Allergies or medical contraindications to NSAIDs

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - From oocyte retrieval day through approximately 5 days until fresh embryo transfer

Participants receive an intravenous dose of Ketorolac or no Ketorolac immediately after oocyte retrieval while still under sedation. IVF care continues as planned including embryo transfer on day 5 post-retrieval.

1 treatment visit and 1 embryo transfer visit

Follow-up

Duration - Up to 40 weeks following embryo transfer

Participants are monitored for pregnancy outcomes, post-operative pain, and other clinical outcomes up to approximately 40 weeks following embryo transfer.

Visits for pregnancy confirmation and outcome monitoring up to 40 weeks

Trial Site Locations

Total: 1 location

1

UI Health Care Center for Advanced Reproductive Care

Iowa City, Iowa, United States, 52245

Actively Recruiting

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Research Team

J

Jessica Kresowik, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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