N/A
N=131
A Study of Continuous Oral Contraceptives and Doxycycline
Contraceptives, Oral
Bottom Line
View on ClinicalTrials.gov: NCT00480532 ↗Enrolled (actual)
131
Serious AEs
0.0%
Results posted
Jan 2013
Primary outcome: Primary: Differences in Bleeding Patterns Between Study Groups. — 26.72; 31.86; 25.69; 18.84 days
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Lybrel (Drug); Doxycycline (Drug); Oracea (Drug); Placebo (Drug); Doxycycline 100bid x5 days at the time of bleeding (Drug); Subantimicrobial doxycycline daily (Drug); placebo daily (Drug)
- Age
- Adult · 18+ yrs
- Sex
- Female
- Sponsor
- Oregon Health and Science University
- Primary completion
- Jan 2010
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Differences in Bleeding Patterns Between Study Groups. |
26.72; 31.86; 25.69; 18.84 | — |
| SECONDARY Subject Satisfaction. |
63.9; 64.2; 72.0; 67.0 | — |
| SECONDARY Subject Compliance |
25; 21; 19; 20 | — |
Summary
The purpose of this study is to learn if the study drug, doxycycline, can decrease the amount of unplanned vaginal bleeding that women commonly experience when taking combined oral contraception (COC)- pills with estrogen and progestin - in a continuous fashion - no hormone-free week. The study drug, doxycycline, is an antibiotic used commonly for many conditions (i.e. acne, Chlamydia infections, pneumonia) and can be safely used on a daily basis. Doxycycline has been shown to decrease unplanned vaginal bleeding in progestin-only contraception but has not been studied in combined hormonal contraception.
Eligibility Criteria
Inclusion Criteria
- General good health
- Willing and able to agree to randomization and sign informed consent
- Currently having regular menstrual cycles (24-36 days), with combined cyclic hormonal method (COCs, Nuva Ring, Ortho Evra), without intermenstrual bleeding in last 2 years.
Exclusion Criteria
- Intrauterine device (IUD) in place
- Abnormal pap smear that has not been treated or followed up
- Those with hypersensitivity reactions to doxycycline or any of the tetracyclines
- Use of depomedroxyprogesterone acetate within 9 months of the start of the study.
- Use of hormonal medications (excluding cyclic contraceptives and plan B) within 2 months of the start of the study.
- Any one unwilling to keep a daily menstrual diary or otherwise unwilling to follow the study criteria
- Currently taking medications that interfere with COCs (rifampin, carbamazepine, St. Johns wort)
- Currently has a progestin implant
- Positive Gonorrhea or Chlamydia cultures at enrollment examination
- Smoking more than 5 cigarettes per month
- Any medical condition that is a contraindication to the use of COCs in accordance with product labeling including:
- History of thrombophlebitis, deep venous thrombosis, thrombogenic vasculopathies, thrombogenic rhythm disorders or thromboembolic disorders
- Current or past history of cerebrovascular or coronary artery disease
- Scheduled major surgery in the next six months with prolonged immobilization
- Diabetes with vascular involvement
- Headache with focal neurologic symptoms
- Uncontrolled hypertension
- Suspected or known carcinoma of the breast or personal history of breast cancer
- Carcinoma of the endometrium or other known or suspected estrogen dependent neoplasms
- Undiagnosed genital bleeding
- History of cholestatic jaundice of pregnancy or cholestatic jaundice with prior oral contraceptive use
- Hepatic adenoma or carcinoma or active liver disease if liver function has not returned to normal
- Known or suspected pregnancy
- Hypersensitivity to estrogen or progesterone containing products
Data sourced from ClinicalTrials.gov (NCT00480532). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.