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Led by Jessica D. Kresowik · Updated on 2025-12-15
200
Participants Needed
1
Research Sites
48 weeks
Total Duration
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 ketorolacs 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 11 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
Ketorolac Use and Fresh Embryo Transfer Outcomes
J
Jessica Kresowik, MD
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Jessica D. Kresowik
Lead Sponsor
This table compares participation in this trial with other options available for this condition. The information is drawn from published research and the trial’s study details and is provided for educational purposes only.
| Factors | IV Ketorolac | Standard Pain Control (No Ketorolac) |
|---|---|---|
| What is it? | IV ketorolac is a nonsteroidal anti-inflammatory drug (NSAID) administered intravenously immediately after oocyte retrieval for pain control. It is being evaluated for its effects on pain and embryo transfer outcomes. | Standard pain control without ketorolac refers to usual pain management after oocyte retrieval, avoiding NSAIDs. This arm serves as the comparator for assessing ketorolac's effect. |
| Role in clinical trial | Investigational active intervention. | Trial comparator, usual pain control without NSAIDs. |
| Primary use | To relieve post-operative pain and assess impact on embryo transfer outcomes following oocyte retrieval in IVF cycles. | To provide pain management with standard practices without ketorolac, serving as the reference group for efficacy and safety outcome measurement. |
| How is it given or performed? | One dose of 30 mg ketorolac is given intravenously immediately after oocyte retrieval. | No IV ketorolac is administered; pain is managed by standard approaches used in IVF without NSAIDs. |
| Evidence status | Ketorolac has demonstrated safety in perioperative settings and published studies suggest no significant negative impact on pregnancy rates when used after oocyte retrieval, though further evaluation is ongoing. The current trial aims to clarify its effect on implantation, pregnancy, and live birth rates in the IVF population. | Standard pain management (no ketorolac) follows typical IVF protocols. No external evidence suggests benefits or risks beyond usual clinical experience. The trial control serves as the benchmark for measuring ketorolac’s effects in this setting. |
| Important limitations | Ketorolac’s impact on fresh embryo transfer outcomes is not fully established. Results are limited to the IVF population and may not generalize to all fertility or surgical patients. The study does not address long-term safety or fertility outcomes beyond live birth. | Standard pain management may vary by clinic. Lack of ketorolac may increase reliance on opioids, which has broader risks such as dependency. Literature indicates post-surgical opioid exposure is a concern for reproductive-age women. |
Disclaimer: This comparison is created with the help of artificial intelligence(AI) and may contain errors or missing information. It is not medical advice and does not mean one option is better or safer than another. Clinical trials are still being studied, and joining a trial is your choice. Please consult your healthcare professional before making any decisions.
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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Lead Sponsor