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- Withdrawn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