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 investigators will conduct a double-blinded, randomized, placebo-controlled, superiority trial of those undergoing D\&E between 16 and 26-weeks gestation at Stanford Health Care to evaluate the following aims: Aim 1: To assess the effect of perioperative dexmedetomidine on validated measures of grief in patients undergoing second-trimester D\&E. Aim 2: To evaluate the feasibility and implementation of perioperative dexmedetomidine within the routine workflow of outpatient OR-based D\&E procedures.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Enrollment
100
Infusion of dexmedetomidine 0.5ug/kg over 10 minutes at anesthesia induction
Saline infusion at equal volume to intervention arm
Stanford Health Care
Palo Alto, California, United States
Reproductive Grief Screen
Validated 5-question survey to evaluate for pathologic grief
Time frame: 2 weeks post-procedure
Edinburgh Postnatal Depression Scale [EDPS]
Validated 10-question tool used to screen for perinatal and postpartum depression
Time frame: 2 weeks post-procedure
PTSD Checklist for DSM-5 (PCL-5)
20-item tool measuring PTSD symptom severity
Time frame: 2 weeks post-procedure
Post-anesthesia care unit (PACU) length of stay
Length of stay (in minutes) will be compared between groups.
Time frame: Immediately post-procedure (up to 6 hours)
Reproductive Grief Screen
Validated 5-question survey to evaluate for pathologic grief
Time frame: 4 weeks post-procedure
Edinburgh Postnatal Depression Scale [EDPS]
Validated 10-question tool used to screen for perinatal and postpartum depression
Time frame: 4 weeks post-procedure
PTSD Checklist for DSM-5 (PCL-5)
20-item tool measuring PTSD symptom severity
Time frame: 4 weeks post-procedure
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.