Trial | NCT03018171  Report issue

Title

Intrathecal Clonidine Addiction for Combined Spinal Epidural Analgesia During Labor
Impact on Maternal and Fetal Wellbeing and on Labor Curve of Intrathecal Clonidine Addiction for Labor Analgesia. A Randomized Controlled Trial.

  • Phase

    Phase 4

  • Study Type

    Interventional

  • Status

    Unknown status

  • Study Participants

    268
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.
Study Started
Jan 31
2017
Primary Completion
Jun 30
2017
Anticipated
Study Completion
Aug 31
2017
Anticipated
Last Update
Apr 27
2017

Drug Clonidine

Intrathecal clonidine addiction

Drug Sufentanil

Intrathecal

SC Experimental

this arm will receive intrathecal clonidine addiction to sufentanil during combined spinal epidural analgesia for labor

S Active Comparator

this arm will receive intrathecal sufentanil during combined spinal epidural analgesia for labor

Criteria 

Inclusion Criteria:

Written maternal informed consent
Singleton pregnancy
Gestational age ≥ 37 weeks,
ASA I
BMI < 30
fetus in cephalic presentation

Exclusion Criteria:

Suspect or certainty of fetal malformation,
Presence of conditions such as preeclampsia, multiparity, preterm labor
History of adverse reaction to α-2 adrenergic agonists
Nicotine addiction
Chronic use of opioid
No Results Posted