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WithdrawnPhase 2/3

Perioperative Dexmedetomidine to Reduce Post-procedure Grief Following Second-trimester Dilation and Evacuation

Key facts

Who runs it
Stanford University
Where
Palo Alto, United StatesSee the site
Trial code
Status
Withdrawn
Phase
Phase 2/3
Started
Jul 2026
Expected to end
Jul 2028
Type of study
Interventional, 2 groupsOne group gets a placebo (a dummy treatment), for comparison.
Treatments tested
  • Dexmedetomidine (IV) 0.5 mcg/kg
  • Placebo
Record updated
17 July 2026
Why it stopped
Lack of funding

Who can take part

Age
18 years and older
Sex
Women only
Healthy volunteers
Cannot take part

The registry criteria, word for word

Show all 6 criteriaShow less

Who can take part

  • English- or Spanish-fluency
  • 16-26 weeks gestation
  • D\&E in the operating room

Who cannot take part

  • Unscheduled or emergent procedure
  • Contraindication to dexmedetomidine per package insert
  • Judgement of clinical anesthesiologist providing care

Where in United States

  • Stanford Health CarePalo Alto, United States

About the trial

What the trial wants to find out

People seeking second-trimester dilation and evacuation (D\&E) procedures are often facing profoundly challenging circumstances, including desired pregnancies complicated by fetal anomalies or demise, serious maternal health conditions, or changes in financial or relationship status. Although abortion regret is uncommon, the emotional burden surrounding these experiences is substantial: many patients experience significant grief and post-traumatic stress symptoms in the weeks to months following care. Perioperative interventions that decrease the body's stress response offer a promising opportunity to reduce downstream psychologic morbidity. Dexmedetomidine has been shown to reduce PTSD symptoms in other high-stress medical and surgical settings. The investigators are undertaking a randomized trial to evaluate whether perioperative administration of dexmedetomidine during second-trimester D\&E can reduce the frequency and severity of post-procedural grief, directly addressing an unmet need in patient-centered, trauma-informed abortion care.

The 2 groups in the trial

  • DexmedetomidineTreatment being tested

    Infused 0.5ug/kg over 10 minutes at anesthesia induction

    Treatment: Dexmedetomidine (IV) 0.5 mcg/kg

  • PlaceboPlacebo, for comparison

    Saline at equal volume to intervention group

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Record updated
17 July 2026