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N/A N=181 Randomized Triple-blind Prevention

A Randomized Controlled Trial of Three Antibiotic Regimens for First Trimester Abortions

First Trimester Abortion

Enrolled (actual)
181
Serious AEs
0.6%
Results posted
Feb 2022
Primary outcome: Primary: Nausea Scale — 8; 9; 6; 6 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Azithromycin (Drug); Doxycycline (Drug); Metronidazole (Drug); Placebo (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
Female
Sponsor
Medstar Health Research Institute
Primary completion
Jul 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Nausea Scale
8; 9; 6; 6; 18; 15
PRIMARY
Emesis Severity
20; 24; 13; 17; 12; 8
SECONDARY
Pain Scale
20; 17; 16; 13; 18; 14
SECONDARY
Serum Antibiotic Levels
0.41; 1.1; 8.2
SECONDARY
Endometrial Growth
4; 7; 8; 1; 3; 4

Summary

This study, a double blinded randomized controlled trial, is being done to compare side effects of commonly used antibiotic regimens prior to same day abortion procedures. In total, 180 pregnant women in their first trimester of pregnancy (5 0/6-13 6/7 weeks gestation) will be randomized to receive one of the three commonly used antibiotics (azithromycin, doxycycline, metronidazole) for same day abortion procedures or placebo prior to their abortion procedure. Approximately, 30-60 mins after study drug administration, the procedure will be performed. A sub-study will be completed on 40 women who consent to endometrial sampling and to have their blood drawn.

Eligibility Criteria

Inclusion Criteria

  • Women in good general health.
  • English speaking.
  • Age 18 or over.
  • Seeking non-urgent surgical termination of pregnancy.
  • Gestational age of 5 0/7 to 13 6/7 weeks, confirmed by sonogram.

Exclusion Criteria

  • Less than 18 years of age.
  • Early pregnancy failure or fetal demise.
  • Poor general health that would prevent one from tolerating the medication or surgical procedure.
  • Intolerance, allergy, or contraindication to any of the study medications.
  • Inability to tolerate oral intake due to current nausea or vomiting.
  • Diagnosis of hyperemesis gravidarum with current pregnancy.
  • Need of an urgent surgical abortion.
  • Gestational age outside of 5-13 6/7 weeks by sonogram.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02756403). 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.

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