The study aims to evaluate the impact of the addition of 20 mcg of intrathecal clonidine in
combined spinalepidural for labor analgesia on the local anesthetic consumption, on labor
performance and on maternal fetal well-being.
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Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Full eligibility criteria for NCT03018171
Ages eligible for Study
18 Years to 40 Years
Genders eligible for Study
Accepts Healthy Volunteers
Written maternal informed consent
Gestational age ≥ 37 weeks,
BMI < 30
fetus in cephalic presentation
Suspect or certainty of fetal malformation,
Presence of conditions such as preeclampsia, multiparity, preterm labor
History of adverse reaction to α-2 adrenergic agonists
Chronic use of opioid
All locations for NCT03018171
San Giovanni Calibita Fatebenefratelli, Tiberine Island, Hospital
Rome, Italy, 00186
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View full eligibility
Tris trial is registered with FDA with number: NCT03018171. The sponsor of the trial is San Giovanni Calibita Fatebenefratelli Hospital and it is looking for 268 volunteers for the current phase.
Official trial title: Impact on Maternal and Fetal Wellbeing and on Labor Curve of Intrathecal Clonidine Addiction for Labor Analgesia. A Randomized Controlled Trial.
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