Actively Recruiting

Phase 2
Age: 18Years - 40Years
FEMALE
Healthy Volunteers
NCT05695352

Oral Levonorgestrel Plus Meloxicam, IG-002 Delays Ovulation in Normal Menstruating Women by Seven Days

Led by InnovaGyn, Inc. · Updated on 2025-08-20

21

Participants Needed

1

Research Sites

178 weeks

Total Duration

On this page

Sponsors

I

InnovaGyn, Inc.

Lead Sponsor

E

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This clinical trial determines if an oral medication taken within 2 days of anticipated ovulation will delay ovulation by 7 days. The study compares oral placebo tablets (control) to oral levonorgestrel, a synthetic hormone, and meloxicam, a non-steroidal anti-inflammatory drug (treatment) in 21 healthy women between the ages of 18 to 40. The control or treatment are taken 48 hours apart in the first and second menstrual cycle, respectively. The first dose is taken when the ovarian follicle has a diameter of 17 mm measured by transvaginal ultrasound. This follicle diameter is found 2 ± 1.0 days before ovulation. Ovulation is determined by a change in urinary hormone levels analyzed in first morning daily urine. The Investigators anticipate that the control cycle will have an interval to ovulation of ≤ 3 days from first placebo to ovulation while a delay of ≥7 days is found between first treatment to ovulation. A second question is to determine the side effects between control versus treatment based on symptoms such as nausea or abdominal cramping, change in blood pressure or pulse rate and the interval in menstrual bleeding. Each study participant has approximately 9 visits during each of two menstrual cycles. The visits between menstrual day 9 (first visit) to largest follicle are 3 to 6 depending upon follicle growth. A blood sample with a transvaginal ultrasound for ovarian follicle diameter is obtained at each visit. The appropriate medication is taken when the ovarian follicle largest diameter is 17 mm. The second dose is taken 2 days later with interim and final visits at 5 and 10 days following first dose. Each participant collects first morning urine from menstrual day 9 to 23. A teaspoonful of morning urine is placed in a storage tube and kept in a refrigerator freezer section until returned at a scheduled visit. All urine samples are kept frozen until analyzed for the metabolites of estrogen and progesterone by a central research laboratory. A change in the ratio of estrogen to progesterone metabolites is indicative of ovulation because more progesterone is secreted after ovulation from the ovary. The primary research outcome compares the interval in days from first dose of medication to ovulation between control and treatment. Secondary outcomes are menstrual cramps, vaginal bleeding, nausea, and headache, and changes in blood pressure, pulse, and interval between menstrual periods in control compared to treatment cycles.

CONDITIONS

Official Title

Oral Levonorgestrel Plus Meloxicam, IG-002 Delays Ovulation in Normal Menstruating Women by Seven Days

Who Can Participate

Age: 18Years - 40Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Female in good general health without chronic medical conditions causing frequent exacerbations
  • Age between 18 to 40 years inclusive at enrollment
  • Body mass index (BMI) 30 kg/m8 or less without recent rapid weight changes
  • Intact uterus with both ovaries intact
  • Pap test within guidelines or performed at screening if 21 years or older
  • Regular menstrual cycles of 24 to 32 days, with specific requirements after pregnancy or abortion
  • Negative urine pregnancy test on menstrual cycle day 9 before treatment
  • Not at risk of pregnancy during study due to abstinence, permanent contraception, non-hormonal IUD, or willingness to use non-hormonal barrier contraception
  • Willing and able to comply with study requirements including daily urine collection
  • Lives within reasonable distance from study site
  • Understands and signs informed consent before screening
  • Agrees not to participate in other clinical trials during this study
  • Screening serum progesterone level greater than 3 ng/ml
Not Eligible

You will not qualify if you...

  • Known allergy or contraindication to progestins
  • Abnormal transvaginal ultrasound or safety lab results deemed clinically significant
  • Known or suspected alcohol or marijuana abuse
  • Undiagnosed abnormal genital bleeding or vaginal abnormalities
  • Uncontrolled thyroid disorder
  • Current use of hormonal contraception or levonorgestrel-releasing IUD
  • Use of long-acting injectable hormonal contraceptive within past 6 months without at least one spontaneous menstrual cycle since
  • Breastfeeding or no spontaneous menstrual bleed since stopping breastfeeding
  • Plans for major surgery or pregnancy during study
  • Smoking more than 15 cigarettes daily or significant e-cigarette nicotine use
  • History or current ischemic heart disease, stroke during pregnancy or hormonal contraception use
  • History or current deep vein thrombosis or thromboembolic disorder
  • Personal or family history of thrombophilia
  • History of retinal vascular lesions or vision loss
  • Known or suspected hormone-sensitive cancers
  • History of other cancers except basal cell carcinoma in remission over 5 years
  • Severe depression not stable on medication or likely worsened by hormonal contraceptives
  • History of headaches with neurological symptoms
  • Current need for hormones or anticoagulants
  • History of cholestatic jaundice or liver disease
  • Elevated blood pressure above specified limits or uncontrolled hypertension
  • Clinically significant abnormal serum chemistry
  • Participation in another clinical trial recently or planned during study
  • Use or planned use of liver enzyme inducers
  • Known HIV infection
  • History of gastrointestinal ulcers or bleeding
  • Use of medications interfering with hormonal contraceptives or NSAIDs or contraindicated in pregnancy
  • Study site staff or close relations with delegated study responsibilities

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Carolina Women's Research and Wellness Center

Raleigh, North Carolina, United States, 27713

Actively Recruiting

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Research Team

D

David F. Archer, MD

CONTACT

W

William L. McPheat, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

TREATMENT

Number of Arms

2

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