Outcomes of Neuraxial Anesthetic Technique on the Trial of Labor After Cesarean (TOLAC)

Completed · Phase 4

Conditions studied: Labor Pain, Complications; Cesarean Section, Pregnancy

In brief

To compare the effects of epidural versus combined spinal and epidural (CSE) anesthesia on the success of Trial of Labor After Cesarean (TOLAC).

Key facts

Study ID

NCT02105558

Run by

The University of Texas Health Science Center, Houston

People needed

46

Starts

2014-04-01

Expected to finish

2017-04-13

Last updated by the study team

2018-07-19

Who can join

Age: 18 and older, up to 50. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• all patients meeting ACOG guidelines for TOLAC
• at least one previous elective cesarean delivery
• <40 weeks gestational age (GA)
• vertex singleton pregnancy with use of continuous fetal monitoring

You may not qualify if…

• Patient refusal of regional anesthetic or with contraindication for regional anesthesia
• BMI >40
• associated comorbidities such as gestational diabetes, preeclampsia, abnormal placentation

Where it is running

• Lyndon B. Johnson Hospital — Houston, Texas, United States

Full record on ClinicalTrials.gov

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